Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter cells and all the future daughter cells. Such abnormal cell proliferation defines the characteristic of what we call cancer. The best example to explain this condition is the mutation in the RAS and MYC proteins.
Normal RAS proteins are GTPases that function in signal transduction from cell surface receptors to the cell’s interior. RAS proteins can be denoted as the binary switches that cycle between ON and OFF states during cellular growth. Usually, these switches are tightly regulated, but in RAS-related diseases such as cancer, the RAS gene mutation or their regulator renders RAS proteins persistently active. For instance, a single amino acid missense mutation in the KRAS protein (a type of RAS protein) impairs its normal functioning. The mutant KRAS cannot be inactivated, leading to continuous growth stimulation. KRAS mutation occurs in 15%- 20% of human cancers, and is most commonly seen in colon cancer, lung cancer, pancreatic cancer, and leukemia.
Abnormal cell proliferation can also occur when mutation results in overexpression of MYC protein. The MYC oncogene belongs to a family of "super-transcription factors" and is deregulated in more than 50% of human cancers. The MYC affects a spectrum of cellular functions, including protein translation, cell cycle progression, ribosome biosynthesis, cell proliferation, differentiation, survival, and immune surveillance.
Du chapitre 34:
Now Playing
34.10 : Abnormal Proliferation
Cell Proliferation
4.3K Vues
34.1 : Qu’est-ce que le cycle cellulaire ?
Cell Proliferation
6.2K Vues
34.2 : Interphase
Cell Proliferation
5.8K Vues
34.3 : Le système de contrôle du cycle cellulaire
Cell Proliferation
6.0K Vues
34.4 : Molécules régulatrices positives
Cell Proliferation
4.2K Vues
34.5 : Inhibition de l’activité CDK
Cell Proliferation
3.3K Vues
34.6 : Le S-CDK initie la réplication de l’ADN
Cell Proliferation
2.0K Vues
34.7 : M-CDK favorise la transition vers la mitose
Cell Proliferation
1.9K Vues
34.8 : Les mitogènes et le cycle cellulaire
Cell Proliferation
3.9K Vues
34.9 : Sénescence cellulaire réplicative
Cell Proliferation
2.4K Vues
34.11 : Les cellules coordonnent la croissance et la prolifération
Cell Proliferation
2.3K Vues
À PROPOS DE JoVE
Copyright © 2025 MyJoVE Corporation. Tous droits réservés.