Krt19⁺/Lgr5⁻ cells are radioresistant cancer-initiating stem cells in the colon and intestine

Date

2015

Authors

Asfaha, S.
Hayakawa, Y.
Muley, A.
Stokes, S.
Graham, T.
Ericksen, R.
Westphalen, C.
Von Burstin, J.
Mastracci, T.
Worthley, D.

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Journal article

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Cell Stem Cell, 2015; 16(6):627-638

Statement of Responsibility

Samuel Asfaha, Yoku Hayakawa, Ashlesha Muley, Sarah Stokes, Trevor A. Graham, Russell E. Ericksen, Christoph B. Westphalen, Johannes von Burstin, Teresa L. Mastracci, Daniel L. Worthley, Chandhan Guha, Michael Quante, Anil K. Rustgi, Timothy C. Wang

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Abstract

Epithelium of the colon and intestine are renewed every 3 days. In the intestine there are at least two principal stem cell pools. The first contains rapid cycling crypt-based columnar (CBC) Lgr5(+) cells, and the second is composed of slower cycling Bmi1-expressing cells at the +4 position above the crypt base. In the colon, however, the identification of Lgr5(-) stem cell pools has proven more challenging. Here, we demonstrate that the intermediate filament keratin-19 (Krt19) marks long-lived, radiation-resistant cells above the crypt base that generate Lgr5(+) CBCs in the colon and intestine. In colorectal cancer models, Krt19(+) cancer-initiating cells are also radioresistant, while Lgr5(+) stem cells are radiosensitive. Moreover, Lgr5(+) stem cells are dispensable in both the normal and neoplastic colonic epithelium, as ablation of Lgr5(+) stem cells results in their regeneration from Krt19-expressing cells. Thus, Krt19(+) stem cells are a discrete target relevant for cancer therapy.

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© 2015 Elsevier Inc.

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