Considerable data support the idea that oncogene-induced senescence remains a barrier that needs to be overcome for malignant transformation of melanocytes. Human nevi stain positive for the senescence-associated β-galactosidase marker, suggesting that cells have lost their proliferative capacity. Most nevi harbor B-RAF or N-RAS mutations, implying that they are growth arrested via oncogene-induced senescence pathways. It remains intriguing how benign nevus cells can escape oncogene-induced senescence for malignant transformation to melanoma. The report by Tran et al. in this issue shows that current senescence markers do not distinguish nevi from melanomas, challenging the notion that nevi are growth-arrested via senescence
International audienceNormal cells possess a limited proliferative life span, after which they enter...
Oncogene-induced senescence is considered to act as a potent barrier to cell transformation, and has...
P>Cell senescence is a permanent growth arrest following extended proliferation. Cultured cancer ...
Cellular senescence permanently restricts the replicative capacity of cells in response to various s...
Cellular senescence permanently restricts the replicative capacity of cells in response to various s...
Melanocytes within benign human nevi are the paradigm for tumor suppressive senescent cells in a pre...
Melanocytes within benign human nevi are the paradigm for tumor suppressive senescent cells in a pre...
Background: Oncogene-induced senescence is considered to act as a potent barrier to cell transformat...
Oncogene-induced senescence is considered to act as a potent barrier to cell transformation, and has...
Mutational activation of the BRAF proto-oncogene in melanocytes reliably produces benign nevi (pigme...
Mutational activation of the BRAF proto-oncogene in melanocytes reliably produces benign nevi (pigme...
Cellular senescence is a stable proliferation arrest associated with an altered secretory pathway (s...
International audienceNormal cells possess a limited proliferative life span, after which they enter...
Cellular senescence is a stable proliferation arrest associated with an altered secretory pathway (s...
International audienceNormal cells possess a limited proliferative life span, after which they enter...
International audienceNormal cells possess a limited proliferative life span, after which they enter...
Oncogene-induced senescence is considered to act as a potent barrier to cell transformation, and has...
P>Cell senescence is a permanent growth arrest following extended proliferation. Cultured cancer ...
Cellular senescence permanently restricts the replicative capacity of cells in response to various s...
Cellular senescence permanently restricts the replicative capacity of cells in response to various s...
Melanocytes within benign human nevi are the paradigm for tumor suppressive senescent cells in a pre...
Melanocytes within benign human nevi are the paradigm for tumor suppressive senescent cells in a pre...
Background: Oncogene-induced senescence is considered to act as a potent barrier to cell transformat...
Oncogene-induced senescence is considered to act as a potent barrier to cell transformation, and has...
Mutational activation of the BRAF proto-oncogene in melanocytes reliably produces benign nevi (pigme...
Mutational activation of the BRAF proto-oncogene in melanocytes reliably produces benign nevi (pigme...
Cellular senescence is a stable proliferation arrest associated with an altered secretory pathway (s...
International audienceNormal cells possess a limited proliferative life span, after which they enter...
Cellular senescence is a stable proliferation arrest associated with an altered secretory pathway (s...
International audienceNormal cells possess a limited proliferative life span, after which they enter...
International audienceNormal cells possess a limited proliferative life span, after which they enter...
Oncogene-induced senescence is considered to act as a potent barrier to cell transformation, and has...
P>Cell senescence is a permanent growth arrest following extended proliferation. Cultured cancer ...