Bu protokol, test edilmiş ve Dr. Richard Hynes (MIT) laboratuvar başlangıçta optimize edilmiştir. Finansman NYSTEM FİKİR ÖDÜLÜ (LX) ve Ruth L. Kirschstein Ulusal Araştırma Hizmet Ödülü (LX) tarafından sağlanmaktadır.

1. Numune Hazırlama <ol><li> ~% 70 büyüme faktörleri veya FBS ile kendi özel medya konfluent (örneğin, MC-1 hücreler için% 10 FBS DMEM) hücreleri büyütün. Plaka medya aspire ve 1 x PBS (8 NaCl Na 2 HPO 4 g / L KCl, 0.2 g / L, 1.15 g / L 0,7 H 2 O, 0.2 g / L KH 2 PO ile hafifçe birkaç kez yıkayın 4, pH 7.3). </li><li> Aspire PBS ve versene% 0.05 tripsin (0.014 g / L fenol kırmızı ve 1 x PBS, pH 7.2 0.2 g / L EDTA-Na) 2 mL ekleyin. Plaka plaka hücre ayrılması kolaylaştırmak için hafifçe sallayın. Hücrelerin mikroskop altında uyun. Genellikle hücreleri ayırmak için 2-5 dakika sürer. </li><li> Tripsin aktivitesi söndürmeye ve 50ml şahin tüp hücreleri toplamak için FBS (veya soya tripsin inhibitörü) içeren medya bol miktarda ekleyin. Hemasitometre kullanarak hücreleri saymak. Temiz bir hemasitometre üzerine hücre süspansiyonu 10μL yükleyin. Ml başına hücre sayısı, ortalama her 10 4 ile çarpılır beş kare içerisinde hücrelerinin eşittir . </li><li> 1000 hücreleri Santrifüj RPM (ya da ~ 200 xg) 3 dakika için bir masa üstü santrifüj. </li><li> Medya hücre pelletini rahatsız etmeden dikkatlice çıkarın. Hanks Dengeli Tampon Çözeltisi (HBSS) ~ 5 x 10 6 hücre / ml son bir konsantrasyona ulaşmak için uygun bir hacim hücreleri tekrar </li><li> Falcon 70 mikron hücre süzgecinden Filtre hücreleri büyük hücreli agrega dışlamak için. Etiketli 5ml Falcon kültür tüpünün üzerinde doğrudan filtre üzerine pipet ucu yerleştirin. Hızla kültür tüpünün içine filtre ile süspansiyon çıkarır. </li><li> Hemasitometre kullanarak tekrar hücre sayımı ve son konsantrasyonu 2.5 x 10 6 / mL seyreltik. Hücreleri buz üzerinde tutun. </li><li> Hücrelerin canlılığı belirleyin. Tripan mavisi ile bazı hücreler Mix ve hemasitometre kullanarak toplam hücreleri üzerinde ölü (mavi) hücrelerinin yüzdesini ölçmek. Hücre canlılığı enjeksiyondan önce ≥% 90 olmalıdır. </li></ol> 2. İntravenöz Enjeksiyon <ol><li> Eldivenleri değiştirin. Yavaşça bir immünyetmezligi fare (çıplak, NOD SCID veya NSG, Jackson Laboratory) kuyruk kapmak ve süzgeç arkasındaki küçük açıklıktan dışarı yapışmasını yarık ve kuyruğunu karşı onun arkasında, fare süzgeç içine onu çekin . </li><li> Halka fare ağız yakalar kez yarık boyunca içe halka yavaşça kaydırın ve yerine kilitleyin. Fare özgürce hareket edebilmek, ancak normal solunum oranına sahip olmalıdır. </li><li> Büyük kuyruk damarlar bul. Dört büyük kan damarlarının bir fare kuyruğu bulunmaktadır. Kuyruk dorsal ve ventral tarafta kan damarları arterler. Damarlar kuyruk yan tarafta. </li><li> 1 ml şırınganın içine hazırlanan hücreler mcL 200&#39;den fazla çizin. 30 G1 / 2 inç iğne takın ve var olabilecek herhangi bir hava kabarcıkları dışarı itmek. Hücrelerin şırınga son hacim 200 mcL (yani, toplam 5 x 10 5 hücreleri) olmalıdır. </li><li> Hücreleri kuyruk damar içine enjekte edilir. <ol class="lalpha"><li> Ilk deneme başarısız olursa, kuyruk daha proksimal bölgeye ikinci bir denemek için kullanılan olabilir, kuyruk distal ucundan başlayın. </li><li> % 70 etanol ile kuyruk silin. Düz kuyruk çekin. Başparmak ile kuyruk ucu tutun ve işaret parmağı ile enjeksiyon noktası desteği. </li><li> Ven iğne takın ve hücreleri enjekte. Iğne ve şırınga enjeksiyon sırasında damar paralel emin olun, aksi takdirde iğne damar duvarı ile karıştırmak ve hücreleri, komşu kuyruk dokulara enjekte. </li><li> Enjeksiyondan sonra iğneyi çekin. Kan, enjeksiyon, enjeksiyon başarıyla giderse bol olmalıdır. Pıhtılaşma kolaylaştırmak için kağıt havlu ya da enjeksiyon yerinde pamuklu temiz bir parça basın ve damar dolaşımı içine herhangi bir kalıntı örnek itin kuyruğu yukarı palpe. </li><li> Süzgeç fareyi bırakın ve kafesine geri dönmek. Bir laboratuar dizüstü (örneğin, kaç denemeler hücreleri enjekte aldı ve ne kadar hücreler enjekte edildi) enjeksiyon işlemi kaydedin. </li><li> Numune Hazırlama Bölümünde açıklandığı gibi, enjeksiyondan sonra hücre canlılığı, belirleyin, 9 adım. Bu adım, hücrelerin enjeksiyon işlemi boyunca hayatta kalmasını güvence sağlar. Bir enjeksiyon deney sonunda, hücre canlılığı azalacak, ancak% 80 üzerinde olmalıdır. </li><li> (Isteğe bağlı) artık hücreleri aşağı Spin ve pelet kez PBS ile yıkayın. Gelecekteki analizler (örneğin, gen ekspresyonu veya knockdowns onaylamak için batı lekeler) -80 ° C&#39;de pelet dondurun. </li></ol></li><li> Genellikle bir veya iki ay sonra, farelerin disseke olacak ve metastaz yerleri kabaca belirlenir. Akciğer, metastaz için birincil site hücreleri sonra ilk karşılaştığınızda bu kapiller yatak içerdiğindendolaşıma girebilir. </li><li> PBS, akciğer (ya da diğer dokular içeren metastaz) her lob ile iyice durulandıktan sonra bir diseksiyon mikroskobu altında (Şekil 1) görülmektedir. Toplam sayısı akciğer metastazları akciğer her iki tarafta saptanabilir metastaz sayısı sayılır ve tüm dört loblar akciğer metastazları sayıları birbirine eklenir. Akciğerlere formalin gecede giderilen eğer 1 akciğer metastazları daha kolay algılanır metastaz bitişik koyu kahverengi akciğer dokusu aksine beyazımsı lekeler olarak apppear beri. </li></ol> 3. Akciğer metastaz Kültürleme Hücreler <ol><li> Akciğer metastazı enjekte edilen farelerin izole edilmiştir. Her biri ayrı kültür olmalıdır. </li><li> Her metastaz 70 mikron hücre süzgecinden (steril) bir iğne kapağı sonuna kadar kıyılmış. </li><li> Orta ve toplanan hücreler bir kültür çanak filtre geçmesine birkaç mL ile hücre süzgeç durulayın. </li><li> Hücreler, rahatsız olmadan en az dört gün boyunca 37 ° C&#39;de inkübe edin. </li><li> Kan veya doku artıkları, tabak PBS ile yıkayın. </li><li> Taze orta ekleyin. Başında, hem kanser hücreleri ve fibroblast hücreleri plakalar üzerinde büyüyecek, ancak yavaş yavaş, fibroblast hücreleri ölecek ve kanser hücreleri tarafından değiştirilmelidir. Kanser hücreleri herhangi bir ilaca dirençli genleri taşıyorsanız, ilgili antibiyotikler ile hücreleri seçin. </li><li> Elde edilen hücrelerin saflık insana özgü proteinlere karşı antikorlar kullanılarak immün değerlendirilir. Biz anti-insan vimentin antikor (NCL-VIM-V9, Novocastra) kullanın. Ilaç seçiminin yokluğunda bile, elde edilen hücrelerin% 99 insan hücreleri üzerinde genellikle içerir. Yeni elde edilen hücrelerin, yukarıda açıklandığı gibi, kendi metastatik yeteneklerini test etmek için bağışık yetmezliği olan farelere tekrar enjekte edilebilir. </li></ol> 4. Temsilcisi Sonuçlar <ol><li> Bu testin sonunda, çok az akciğer metastazı kötü metastatik kanser hücre hattı gelecek bir çok metastatik kanser hücre hattı genellikle birçok akciğer metastazı (Şekil 1), 1 yol açmaktadır. </li><li> Bu yöntemi kullanarak elde edilen hücreler genellikle ebeveyn hat, yine bu testte kullanılarak test daha fazla metastaz neden olmaktadır. 1-3 </li></ol><img src="/files/ftp_upload/1942/1942fig1.jpg" alt="Şekil 1" /> Şekil 1, kanser hücrelerinin kuyruk damar enjeksiyondan sonra fare akciğerlerin Temsilcisi görüntüler . Insan metastatik melanom hücre hattı, SM hücreleri, 4, 5 x 10 5, bağışık yetmezliği olan farelere kuyruk damar içine enjekte edildi. İki ay sonra, akciğerler izole edildi ve metastaz normal akciğer dokusu arasında dağılmış bulundu.

<ol>
	<li>Xu, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gene+expression+changes+in+an+animal+melanoma+model+correlate+with+aggressiveness+of+human+melanoma+metastases.">Gene expression changes in an animal melanoma model correlate with aggressiveness of human melanoma metastases.</a> Mol Cancer Res. 6 (5), 760-760 (2008).</li><li>Clark, E. A., Golub, T. R., Lander, E. S., Hynes, R. O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genomic+analysis+of+metastasis+reveals+an+essential+role+for+RhoC.">Genomic analysis of metastasis reveals an essential role for RhoC.</a> Nature. 406 (6795), 532-532 (2000).</li><li>Xu, L., Begum, S., Hearn, J. D., Hynes, R. O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=GPR56,+an+atypical+G+protein-coupled+receptor,+binds+tissue+transglutaminase,+TG2,+and+inhibits+melanoma+tumor+growth+and+metastasis.">GPR56, an atypical G protein-coupled receptor, binds tissue transglutaminase, TG2, and inhibits melanoma tumor growth and metastasis.</a> Proc Natl Acad Sci U S A. 103 (24), 9023-9023 (2006).</li><li>Kozlowski, J. M., Hart, I. R., Fidler, I. J., Hanna, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+human+melanoma+line+heterogeneous+with+respect+to+metastatic+capacity+in+athymic+nude+mice.">A human melanoma line heterogeneous with respect to metastatic capacity in athymic nude mice.</a> J Natl Cancer Inst. 72 (4), 913-913 (1984).</li><li>Kang, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+multigenic+program+mediating+breast+cancer+metastasis+to+bone.">A multigenic program mediating breast cancer metastasis to bone.</a> Cancer Cell. 3 (6), 537-537 (2003).</li></ol>

Metastaz, kanser hastalarının ölüm önde gelen nedenidir. Birincil lokusların, dolaşıma giriş (intravasation), dolaşım (ekstravazasyonu) çıkış, ve uzak bir organ hayatta kalma ve büyüme kanser hücrelerinin ayrılması: Bu dört ana adımdan oluşur. Insan metastaz yavaş bir süreç olarak görülür ve genellikle gecikme yıl sonra tezahür eder. Zamanında ilerlemesi çalışma için, yukarıdaki nispeten hızlı deneysel assay bağışık yetmezliği olan farelere kurulmuştur 4 Kurulduğu...

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		<th>Catalogue Number</th>
		<th>Comment</th>
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<tr>
<td>DMEM</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>10313-021</td>
<td>&nbsp;</td>
<tr>
<td>FBS</td>
<td>&nbsp;</td>
<td>Hyclone</td>
<td>SH30088.03</td>
<td>&nbsp;</td>
<tr>
<td>HBSS</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>14175-095</td>
<td>&nbsp;</td>
<tr>
<td>NaCl</td>
<td>&nbsp;</td>
<td>Sigma-Aldrich</td>
<td>S9888</td>
<td>&nbsp;</td>
<tr>
<td>KCl</td>
<td>&nbsp;</td>
<td>Mallinckrodt Chemicals</td>
<td>6838-04</td>
<td>&nbsp;</td>
<tr>
<td>Na2 HPO4.7H2O</td>
<td>&nbsp;</td>
<td>Mallinckrodt Chemicals</td>
<td>7896-04</td>
<td>&nbsp;</td>
<tr>
<td>KH2PO4</td>
<td>&nbsp;</td>
<td>Mallinckrodt Chemicals</td>
<td>7100-12</td>
<td>&nbsp;</td>
<tr>
<td>Phenol red</td>
<td>&nbsp;</td>
<td>Sigma-Aldrich</td>
<td>P3532</td>
<td>&nbsp;</td>
<tr>
<td>EDTA-Na</td>
<td>&nbsp;</td>
<td>EMD Biosciences</td>
<td>4010</td>
<td>&nbsp;</td>
<tr>
<td>Trypan Blue</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>15250-061</td>
<td>&nbsp;</td>
<tr>
<td>Trypsin 2.5%</td>
<td>&nbsp;</td>
<td>Invitrogen</td>
<td>15090-046</td>
<td>&nbsp;</td>
<tr>
<td>Ethanol</td>
<td>&nbsp;</td>
<td>Ultrapure</td>
<td>200-CSGP</td>
<td>&nbsp;</td>
<tr>
<td>50 ml Falcon Tube</td>
<td>&nbsp;</td>
<td>VWR</td>
<td>89039-656</td>
<td>&nbsp;</td>
<tr>
<td>Microcentrifuge Tubes</td>
<td>&nbsp;</td>
<td>Axygen Scientific</td>
<td>MCT-175-C</td>
<td>&nbsp;</td>
<tr>
<td>Falcon 70&#181;m Cell Strainer</td>
<td>&nbsp;</td>
<td>BD Biosciences</td>
<td>352350</td>
<td>&nbsp;</td>
<tr>
<td>5ml Falcon Culture Tube</td>
<td>&nbsp;</td>
<td>VWR</td>
<td>60818-576</td>
<td>&nbsp;</td>
<tr>
<td>Hemacytometer</td>
<td>&nbsp;</td>
<td>Hausser Scientific</td>
<td>15170-208</td>
<td>&nbsp;</td>
<tr>
<td>1 ml syringe</td>
<td>&nbsp;</td>
<td>BD Biosciences</td>
<td>329650</td>
<td>&nbsp;</td>
<tr>
<td>30 &frac12; gauge needle</td>
<td>&nbsp;</td>
<td>BD Biosciences</td>
<td>305106</td>
<td>&nbsp;</td>
<tr>
<td>Mouse restrainer</td>
<td>&nbsp;</td>
<td>Plas Labs Inc.</td>
<td>551-BSRR</td>
<td>&nbsp;</td>
<tr>
<td>Surgical scissors</td>
<td>&nbsp;</td>
<td>Fisher Scientific</td>
<td>08-940</td>
<td>&nbsp;</td>
<tr>
<td>Forceps</td>
<td>&nbsp;</td>
<td>Fisher Scientific</td>
<td>08-902</td>
<td>&nbsp;</td>
<tr>
<td>Dissecting Microscope</td>
<td>&nbsp;</td>
<td>Nikon</td>
<td>SMZ1500</td>
<td>&nbsp;</td>
<tr>
<td>Benchtop Centrifuge</td>
<td>&nbsp;</td>
<td>Thermoscientific</td>
<td>75003491</td>
<td>&nbsp;</td>		</tbody>
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experimental metastasis assay

Metastaz, kanser hastalarının ölüm önde gelen nedenidir. Metastaz mekanizmasını anlamak için, deneysel bir metastaz tahlil bağışık yetmezliği olan farelere kullanılarak kurulmuştur. Bu makale, numune hazırlama, intravenöz enjeksiyon ve akciğer metastaz hücreleri kültür de dahil olmak üzere, bu testte yer alan usul çizmektedir. Kısaca, insan kanser hücreleri önceden belirlenmiş bir sayı hazırlanmıştır.<em&gt; In vitro</em&gt; Ve doğrudan dolaşıma kuyruk damarları aracılığıyla bağışık yetmezliği olan farelere enjekte edildi. Küçük bir hücre sayısı dolaşımda türbülans gibi akciğer gibi iç organlarda metastaz olarak hayatta kalmak ve büyümek. Enjekte edilen farelerin belirli bir süre sonra disseke edilir. Diseksiyon mikroskobu altında metastaz doku dağılımı belirlenir. Belirli bir doku metastaz sayısı ve enjekte edilen kanser hücrelerinin metastatik yeteneği ile doğrudan ilişkilidir. Ortaya metastaz izole ve kültür<em&gt; In vitro</em&gt; Olarak, bağışık yetmezliği olan farelere tekrar enjekte çoğu ebeveyn hat daha gelişmiş metastatik yetenekleri hücre hatları. Bu son derece metastatik türevleri metastatik ilerlemesi düzenleyen genleri veya moleküler yollar tanımlamak için yararlı araçlar haline gelir.

Watch this Scientific Journal Video about Experimental Metastasis Assay at JoVE.com

Experimental Metastasis Assay

Bu makale, insan kanser hücre hatları metastatik potansiyelini belirlemek için kullanılan deneysel bir metastaz testinin prosedürleri açıklamaktadır.

Deneysel metastaz Testi

Metastasis is the leading cause of death in cancer patients.  To understand the mechanism of metastasis, an experimental metastasis assay was established ...

Research

JoVE Journal

Medicine

20.2K Görüntüleme.  University of Rochester Medical Center. Bu makale, insan kanser hücre hatları metastatik potansiyelini belirlemek için kullanılan deneysel bir metastaz testinin prosedürleri açıklamaktadır.

Video: Experimental Metastasis Assay

Quantitative Analysis of Cancer Metastasis using an Avian Embryo Model

During metastasis cancer cells disseminate from the primary tumor, invade into surrounding tissues, and spread to distant organs. Metastasis is a complex process that can involve many tissue types, span variable time periods, and often occur deep within organs, making it difficult to investigate and quantify. In addition, the efficacy of the metastatic process is influenced by multiple steps in the metastatic cascade making it difficult to evaluate the contribution of a single aspect of tumor cell behavior. As a consequence, metastasis assays are frequently performed in experimental animals to provide a necessarily realistic context in which to study metastasis. Unfortunately, these models are further complicated by their complex physiology. The chick embryo is a unique in vivo model that overcomes many limitations to studying metastasis, due to the accessibility of the chorioallantoic membrane (CAM), a well-vascularized extra-embryonic tissue located underneath the eggshell that is receptive to the xenografting of tumor cells (figure 1). Moreover, since the chick embryo is naturally immunodeficient, the CAM readily supports the engraftment of both normal and tumor tissues. Most importantly, the avian CAM successfully supports most cancer cell characteristics including growth, invasion, angiogenesis, and remodeling of the microenvironment. This makes the model exceptionally useful for the investigation of the pathways that lead to cancer metastasis and to predict the response of metastatic cancer to new potential therapeutics. The detection of disseminated cells by species-specific Alu PCR makes it possible to quantitatively assess metastasis in organs that are colonized by as few as 25 cells. Using the Human Epidermoid Carcinoma cell line (HEp3) we use this model to analyze spontaneous metastasis of cancer cells to distant organs, including the chick liver and lung. Furthermore, using the Alu-PCR protocol we demonstrate the sensitivity and reproducibility of the assay as a tool to analyze and quantitate intravasation, arrest, extravasation, and colonization as individual elements of metastasis.

Using quantitative PCR, we demonstrate how the well-established chick CAM model can be used to quantitatively analyze the metastasis of human tumor cells to distant organs.

Kuş Embriyo Model kullanarak Kanser metastaz Kantitatif Analiz

During metastasis cancer cells disseminate from the primary tumor, invade into surrounding tissues, and spread to distant organs. Metastasis is a complex ...

Tıp

In vitro Mesothelial Clearance Assay that Models the Early Steps of Ovarian Cancer Metastasis

Ovarian cancer is the fifth leading cause of cancer related deaths in the United States1. Despite a positive initial response to therapies, 70 to 90 percent of women with ovarian cancer develop new metastases, and the recurrence is often fatal2. It is, therefore, necessary to understand how secondary metastases arise in order to develop better treatments for intermediate and late stage ovarian cancer. Ovarian cancer metastasis occurs when malignant cells detach from the primary tumor site and disseminate throughout the peritoneal cavity. The disseminated cells can form multicellular clusters, or spheroids, that will either remain unattached, or implant onto organs within the peritoneal cavity3 (Figure 1, Movie 1). 
All of the organs within the peritoneal cavity are lined with a single, continuous, layer of mesothelial cells4-6 (Figure 2). However, mesothelial cells are absent from underneath peritoneal tumor masses, as revealed by electron micrograph studies of excised human tumor tissue sections3,5-7 (Figure 2). This suggests that mesothelial cells are excluded from underneath the tumor mass by an unknown process. 
Previous in vitro experiments demonstrated that primary ovarian cancer cells attach more efficiently to extracellular matrix than to mesothelial cells8, and more recent studies showed that primary peritoneal mesothelial cells actually provide a barrier to ovarian cancer cell adhesion and invasion (as compared to adhesion and invasion on substrates that were not covered with mesothelial cells)9,10. This would suggest that mesothelial cells act as a barrier against ovarian cancer metastasis. The cellular and molecular mechanisms by which ovarian cancer cells breach this barrier, and exclude the mesothelium have, until recently, remained unknown. 
Here we describe the methodology for an in vitro assay that models the interaction between ovarian cancer cell spheroids and mesothelial cells in vivo (Figure 3, Movie 2). Our protocol was adapted from previously described methods for analyzing ovarian tumor cell interactions with mesothelial monolayers8-16, and was first described in a report showing that ovarian tumor cells utilize an integrin &#x2013;dependent activation of myosin and traction force to promote the exclusion of the mesothelial cells from under a tumor spheroid17. This model takes advantage of time-lapse fluorescence microscopy to monitor the two cell populations in real time, providing spatial and temporal information on the interaction. The ovarian cancer cells express red fluorescent protein (RFP) while the mesothelial cells express green fluorescent protein (GFP). RFP-expressing ovarian cancer cell spheroids attach to the GFP-expressing mesothelial monolayer. The spheroids spread, invade, and force the mesothelial cells aside creating a hole in the monolayer. This hole is visualized as the negative space (black) in the GFP image. The area of the hole can then be measured to quantitatively analyze differences in clearance activity between control and experimental populations of ovarian cancer and/ or mesothelial cells. This assay requires only a small number of ovarian cancer cells (100 cells per spheroid X 20-30 spheroids per condition), so it is feasible to perform this assay using precious primary tumor cell samples. Furthermore, this assay can be easily adapted for high throughput screening.

In vitro Mesothelial Clearance Assay that Models the Early Steps of Ovarian Cancer Metastasis

The mesothelial clearance assay described here takes advantage of fluorescently labeled cells and time-lapse video microscopy to visualize and quantitatively measure the interactions of ovarian cancer multicellular spheroids and mesothelial cell monolayers. This assay models the early steps of ovarian cancer metastasis.

In vitro Mezotelyal Gümrükleme Assay o Yumurtalık Kanseri Metastaz Erken Adımlar modeller

Ovarian cancer is the fifth leading cause of cancer related deaths in the United States1. Despite a positive initial response to therapies, 70 to 90 ...

Models of Bone Metastasis

Bone metastases are a common occurrence in several malignancies, including breast, prostate, and lung. Once established in bone, tumors are responsible for significant morbidity and mortality1. Thus, there is a significant need to understand the molecular mechanisms controlling the establishment, growth and activity of tumors in bone. Several in vivo models have been established to study these events and each has specific benefits and limitations. The most commonly used model utilizes intracardiac inoculation of tumor cells directly into the arterial blood supply of athymic (nude) BalbC mice. This procedure can be applied to many different tumor types (including PC-3 prostate cancer, lung carcinoma, and mouse mammary fat pad tumors); however, in this manuscript we will focus on the breast cancer model, MDA-MB-231. In this model we utilize a highly bone-selective clone, originally derived in Dr. Mundy's group in San Antonio2, that has since been transfected for GFP expression and re-cloned by our group3. This clone is a bone metastatic variant with a high rate of osteotropism and very little metastasis to lung, liver, or adrenal glands. While intracardiac injections are most commonly used for studies of bone metastasis2, in certain instances intratibial4 or mammary fat pad injections are more appropriate. Intracardiac injections are typically performed when using human tumor cells with the goal of monitoring later stages of metastasis, specifically the ability of cancer cells to arrest in bone, survive, proliferate, and establish tumors that develop into cancer-induced bone disease. Intratibial injections are performed if focusing on the relationship of cancer cells and bone after a tumor has metastasized to bone, which correlates roughly to established metastatic bone disease. Neither of these models recapitulates early steps in the metastatic process prior to embolism and entry of tumor cells into the circulation. If monitoring primary tumor growth or metastasis from the primary site to bone, then mammary fat pad inoculations are usually preferred; however, very few tumor cell lines will consistently metastasize to bone from the primary site, with 4T1 bone-preferential clones, a mouse mammary carcinoma, being the exception 5,6.
This manuscript details inoculation procedures and highlights key steps in post inoculation analyses. Specifically, it includes cell culture, tumor cell inoculation procedures for intracardiac and intratibial inoculations, as well as brief information regarding weekly monitoring by x-ray, fluorescence and histomorphometric analyses.

Animal models are frequently utilized to study cancer metastasis to bone. In this protocol we will describe two common methods of tumor inoculation for bone metastasis studies and briefly describe some of the analyses utilized to monitor and quantify these models.

Kemik Metastaz Modelleri

Bone metastases are a common occurrence in several malignancies, including breast, prostate, and lung. Once established in bone, tumors are responsible ...

Experimental Human Pneumococcal Carriage

Experimental human pneumococcal carriage (EHPC) is scientifically important because nasopharyngeal carriage of Streptococcus pneumoniae is both the major source of transmission and the prerequisite of invasive disease. A model of carriage will allow accurate determination of the immunological correlates of protection, the immunizing effect of carriage and the effect of host pressure on the pathogen in the nasopharyngeal niche. Further, methods of carriage detection useful in epidemiologic studies, including vaccine studies, can be compared.
Aim
We aim to develop an EHPC platform that is a safe and useful reproducible method that could be used to down-select candidate novel pneumococcal vaccines with prevention of carriage as a surrogate of vaccine induced immunity. It will work towards testing of candidate vaccines and descriptions of the mechanisms underlying EHPC and vaccine protection from carriage1. Current conjugate vaccines against pneumococcus protect children from invasive disease although new vaccines are urgently needed as the current vaccine does not confer optimal protection against non-bacteraemic pneumonia and there has been evidence of serotype replacement with non-vaccine serotypes2-4.
Method
We inoculate with S. pneumoniae suspended in 100 &mu;l of saline. Safety is a major factor in the development of the EHPC model and is achieved through intensive volunteer screening and monitoring. A safety committee consisting of clinicians and scientists that are independent from the study provides objective feedback on a weekly basis.
The bacterial inoculum is standardized and requires that no animal products are inoculated into volunteers (vegetable-based media and saline). The doses required for colonization (104-105) are much lower than those used in animal models (107)5. Detecting pneumococcal carriage is enhanced by a high volume (ideally &gt;10 ml) nasal wash that is relatively mucus free. This protocol will deal with the most important parts of the protocol in turn. These are (a) volunteer selection, (b) pneumococcal inoculum preparation, (c) inoculation, (d) follow-up and (e) carriage detection.
Results
Our current protocol has been safe in over 100 volunteers at a range of doses using two different bacterial serotypes6. A dose ranging study using S. pneumoniae 6B and 23F is currently being conducted to determine the optimal inoculation dose for 50% carriage. A predicted 50% rate of carriage will allow the EHPC model to have high sensitivity for vaccine efficacy with small study numbers.

Experimental human pneumococcal carriage offers a natural model of carriage and a potential model for use in vaccine development. This technique is valuable yet complex and involves clinical risk by introducing a pathogen into a human. We have developed a detailed protocol.

Deneysel İnsan Pnömokok Taşıma

Experimental human pneumococcal carriage (EHPC) is scientifically important because nasopharyngeal carriage of Streptococcus pneumoniae is both the major ...

The In ovo CAM-assay as a Xenograft Model for Sarcoma

Sarcoma is a very rare disease that is heterogeneous in nature, all hampering the development of new therapies. Sarcoma patients are ideal candidates for personalized medicine after stratification, explaining the current interest in developing a reproducible and low-cost xenotransplant model for this disease. The chick chorioallantoic membrane is a natural immunodeficient host capable of sustaining grafted tissues and cells without species-specific restrictions. In addition, it is easily accessed, manipulated and imaged using optical and fluorescence stereomicroscopy. Histology further allows detailed analysis of heterotypic cellular interactions.
This protocol describes in detail the in ovo grafting of the chorioallantoic membrane with fresh sarcoma-derived tumor tissues, their single cell suspensions, and permanent and transient fluorescently labeled established sarcoma cell lines (Saos-2 and SW1353). The chick survival rates are up to 75%. The model is used to study graft- (viability, Ki67 proliferation index, necrosis, infiltration) and host (fibroblast infiltration, vascular ingrowth) behavior. For localized grafting of single cell suspensions, ECM gel provides significant advantages over inert containment materials. The Ki67 proliferation index is related to the distance of the cells from the surface of the CAM and the duration of application on the CAM, the latter determining a time frame for the addition of therapeutic products.

The In ovo CAM-assay as a Xenograft Model for Sarcoma

The in ovo chorioallantoic membrane (CAM) is grafted with fresh sarcoma-derived tumor tissues, their single cell suspensions, and permanent and transient fluorescently labeled established sarcoma cell lines. The model is used to study graft- (viability, Ki67 proliferation index, necrosis, infiltration) and host (fibroblast infiltration, vascular ingrowth) behavior.

<em&gt; Ovo</emSarkoma için bir Xenograftmodel olarak&gt; CAM-testi

Sarcoma is a very rare disease that is heterogeneous in nature, all hampering the development of new therapies. Sarcoma patients are ideal candidates for ...

An Orthotopic Murine Model of Human Prostate Cancer Metastasis

Our laboratory has developed a novel orthotopic implantation model of human prostate cancer (PCa). As PCa death is not due to the primary tumor, but rather the formation of distinct metastasis, the ability to effectively model this progression pre-clinically is of high value. In this model, cells are directly implanted into the ventral lobe of the prostate in Balb/c athymic mice, and allowed to progress for 4-6 weeks. At experiment termination, several distinct endpoints can be measured, such as size and molecular characterization of the primary tumor, the presence and quantification of circulating tumor cells in the blood and bone marrow, and formation of metastasis to the lung. In addition to a variety of endpoints, this model provides a picture of a cells ability to invade and escape the primary organ, enter and survive in the circulatory system, and implant and grow in a secondary site. This model has been used effectively to measure metastatic response to both changes in protein expression as well as to response to small molecule therapeutics, in a short turnaround time.

This orthotopic model of human prostate cancer allows for quantification of tumor size, circulating tumor cells, and formation of distinct metastasis to the lung. As cells must escape the primary organ, enter the blood stream, and implant into a secondary site, this model effectively recapitulates the scenario in humans.

İnsan Prostat Kanser metastaz Ortotopik fare modeli

Our laboratory has developed a novel orthotopic implantation model of  human prostate cancer (PCa). As PCa death is not due to the primary tumor, but  ...

Primary Tumor and MEF Cell Isolation to Study Lung Metastasis

In breast tumorigenesis, the metastatic stage of the disease poses the greatest threat to the affected individual. Normal breast cells with altered genotypes now possess the ability to invade and survive in other tissues. In this protocol, mouse mammary tumors are removed and primary cells are prepared from tumors. The cells isolated from this procedure are then available for gene profiling experiments. For successful metastasis, these cells must be able to intravasate, survive in circulation, extravasate to distant organs, and survive in that new organ system. The lungs are the typical target of breast cancer metastasis. A set of genes have been discovered that mediates the selectivity of metastasis to the lung. Here we describe a method of studying lung metastasis from a genetically engineered mouse model.. Furthermore, another protocol for analyzing mouse embryonic fibroblasts (MEFs) from the mouse embryo is included. MEF cells from the same animal type provide a clue of non-cancer cell gene expression. Together, these techniques are useful in studying mouse mammary tumorigenesis, its associated signaling mechanisms and pathways of the abnormalities in embryos.

The goal of this protocol is to study breast tumorigenesis. With this technique, mouse mammary tumors are removed and primary cells are prepared from tumors. A lung extraction protocol is included for studying lung metastasis. Furthermore, another protocol for analyzing mouse embryonic fibroblasts from the mouse embryo is included.

Primer Tümör ve Akciğer Metastazı Eğitim için MEF Hücre İzolasyonu

In breast tumorigenesis, the metastatic stage of the disease poses the greatest threat to the affected individual. Normal breast cells with altered ...

Chick Heart Invasion Assay for Testing the Invasiveness of Cancer Cells and the Activity of Potentially Anti-invasive Compounds

The goal of the chick heart assay is to offer a relevant organ culture method to study tumor invasion in three dimensions. The assay can distinguish between invasive and non-invasive cells, and enables study of the effects of test compounds on tumor invasion. Cancer cells - either as aggregates or single cells - are confronted with fragments of embryonic chick heart. After organ culture in suspension for a few days or weeks the confronting cultures are fixed and embedded in paraffin for histological analysis. The three-dimensional interaction between the cancer cells and the normal tissue is then reconstructed from serial sections stained with hematoxylin-eosin or after immunohistochemical staining for epitopes in the heart tissue or the confronting cancer cells. The assay is consistent with the recent concept that cancer invasion is the result of molecular interactions between the cancer cells and their neighbouring stromal host elements (myofibroblasts, endothelial cells, extracellular matrix components, etc.). Here, this stromal environment is offered to the cancer cells as a living tissue fragment. Supporting aspects to the relevance of the assay are multiple. Invasion in the assay is in accordance with the criteria of cancer invasion: progressive occupation and replacement in time and space of the host tissue, and invasiveness and non-invasiveness in vivo of the confronting cells generally correlates with the outcome of the assay. Furthermore, the invasion pattern of cells in vivo, as defined by pathologists, is reflected in the histological images in the assay. Quantitative structure-activity relation (QSAR) analysis of the results obtained with numerous potentially anti-invasive organic congener compounds allowed the study of structure-activity relations for flavonoids and chalcones, and known anti-metastatic drugs used in the clinic (e.g., microtubule inhibitors) inhibit invasion in the assay as well. However, the assay does not take into account immunological contributions to cancer invasion.

Here, we present a protocol to study the invasion of tumor cells into living normal tissue fragments in three dimensions. This organ culture technique is mainly applied to test potentially anti-invasive drugs in vitro.

Test Chick Kalp Invasion Testi Kanser hücrelerinin invazivliğini ve Potansiyel Anti-invaziv Bileşikler Etkinlik

The goal of the chick heart assay is to offer a relevant organ culture method to study tumor invasion in three dimensions. The assay can distinguish ...

A "Patient-Like" Orthotopic Syngeneic Mouse Model of Hepatocellular Carcinoma Metastasis

The majority of cancer-related deaths are caused by the metastasis of the cancer rather than the primary tumor itself. Yet, the underlying mechanisms of cancer metastasis are still unclear. Animal models are essential for elucidating the mechanisms and for evaluating novel strategies for the treatment of metastatic cancers. Here, an in-depth description of a &#8220;patient-like&#8221; orthotopic syngeneic mouse model for exploring the mechanisms of metastasis of solid organ tumors is provided. The survival surgical implantation of BNL 1ME A.7R.1 mouse hepatocellular carcinoma cells directly into the liver (the organ of origin) of the inbred wild-type immune competent laboratory mouse strain, BALB/c is described. The success and reproducibility of this methodology recommends it for widespread use in elucidating the biological mechanisms of solid organ cancer metastasis.

A &quot;Patient-Like&quot; Orthotopic Syngeneic Mouse Model of Hepatocellular Carcinoma Metastasis

The metastatic spread of cancer is the major cause of cancer-related deaths. We provide an in-depth description of our survival surgery methodology for establishing a &#8220;patient-like&#8221; orthotopic syngeneic mouse model system for studying the mechanisms of metastasis in solid organ tumors.

Bir &quot;Hasta gibi&quot; Ortotopik singenik Fare Modeli Hepatoselüler karsinomu metastazı

The majority of cancer-related deaths are caused by the metastasis of the cancer rather than the primary tumor itself. Yet, the underlying mechanisms of ...

Quantitation of Intra-peritoneal Ovarian Cancer Metastasis

Epithelial ovarian cancer (EOC) is the leading cause of death from gynecologic malignancy in the United States. Mortality is due to diagnosis of 75% of women with late stage disease, when metastasis is already present. EOC is characterized by diffuse and widely disseminated intra-peritoneal metastasis. Cells shed from the primary tumor anchor in the mesothelium that lines the peritoneal cavity as well as in the omentum, resulting in multi-focal metastasis, often in the presence of peritoneal ascites. Efforts in our laboratory are directed at a more detailed understanding of factors that regulate EOC metastatic success. However, quantifying metastatic tumor burden represents a significant technical challenge due to the large number, small size and broad distribution of lesions throughout the peritoneum. Herein we describe a method for analysis of EOC metastasis using cells labeled with red fluorescent protein (RFP) coupled with in vivo multispectral imaging. Following intra-peritoneal injection of RFP-labelled tumor cells, mice are imaged weekly until time of sacrifice. At this time, the peritoneal cavity is surgically exposed and organs are imaged in situ. Dissected organs are then placed on a labeled transparent template and imaged ex vivo. Removal of tissue auto-fluorescence during image processing using multispectral unmixing enables accurate quantitation of relative tumor burden. This method has utility in a variety of applications including therapeutic studies to evaluate compounds that may inhibit metastasis and thereby improve overall survival.

Ovarian cancer metastasis is characterized by numerous diffuse intra-peritoneal lesions, such that accurate visual quantitation of tumor burden is challenging. Herein we describe a method for in situ and ex vivo quantitation of metastatic tumor burden using red fluorescent protein (RFP)-labeled tumor cells and optical imaging.

İçi periton Yumurtalık Kanseri Metastaz kantitasyonu

Epithelial ovarian cancer (EOC) is the leading cause of death from gynecologic malignancy in the United States.  Mortality is due to diagnosis of 75% of ...