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Journal ArticleDOI

Tracing the cellular origin of cancer

Cédric Blanpain
- 01 Feb 2013 - 
- Vol. 15, Iss: 2, pp 126-134
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TLDR
This review explores how mouse genetic lineage-tracing experiments that allow the expression of oncogenes and/or the deletion of tumour suppressor genes in defined cell lineages have been instrumental in defining the cellular origin of different solid tumours in mouse models for various human cancers.
Abstract
Although many genes that lead to different types of cancer when mutated have been identified, the cells that initiate tumour formation following accumulation of these mutations have, until recently, remained elusive. This review explores how mouse genetic lineage-tracing experiments that allow the expression of oncogenes and/or the deletion of tumour suppressor genes in defined cell lineages have been instrumental in defining the cellular origin of different solid tumours in mouse models for various human cancers.

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Citations
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Dedifferentiation of committed epithelial cells into stem cells in vivo

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Cancer Stem Cells: Basic Concepts and Therapeutic Implications

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Defining the Hallmarks of Metastasis

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References
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Journal ArticleDOI

Defining the origins of Ras/p53-mediated squamous cell carcinoma

TL;DR: Data demonstrate that SCCs can originate from inside the hair follicle stem cell (SC) niche or from immediate progenitors, whereas more developmentally restricted progeny, the transit amplifying (TA) cells, are unable to generate even benign tumors in the same genetic context.
Journal ArticleDOI

Patched1 functions as a gatekeeper by promoting cell cycle progression.

TL;DR: The data suggest that Ptch1 likely functions as a tumor suppressor by inhibiting G1-S phase and G2-M phase cell cycle progression, and the rapid onset of tumor progression clearly indicates Ptch 1 functions as an "gatekeeper."
Journal ArticleDOI

Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers.

TL;DR: The study in hereditary breast cancer tumors analyzing 37 immunohistochemical markers defines the molecular differences between BRCA1 and BRCa2 tumors with respect to hormonal receptors, cell cycle, apoptosis and basal cell markers.
Journal ArticleDOI

The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted

TL;DR: Benign tumours that are at a risk of malignant conversion are primarily derived from cells located within the hair follicle, and the nature of the cell in which tumour initiation occurs is a major determinant of malign potential.
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Trending Questions (1)
Cancer is traced from when?

The paper does not explicitly mention when cancer is traced from. The paper discusses the cellular origin of cancer and how mouse genetic lineage-tracing experiments have helped in identifying the cells that initiate tumor formation.