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BEX2 is required for maintaining dormant cancer stem cell in hepatocellular carcinoma

Cancer stem cells (CSCs) are responsible for therapy resistance and share several properties with normal stem cells. Here, we show that brain‐expressed X‐linked gene 2 (BEX2), which is essential for dormant CSCs in cholangiocarcinoma, is highly expressed in human hepatocellular carcinoma (HCC) lesio...

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Detalles Bibliográficos
Autores principales: Fukushi, Daisuke, Shibuya‐Takahashi, Rie, Mochizuki, Mai, Fujimori, Haruna, Kogure, Takayuki, Sugai, Takahiro, Iwai, Wataru, Wakui, Yuta, Abue, Makoto, Murakami, Kazuhiro, Nakamura, Yasuhiro, Yasuda, Jun, Yamaguchi, Kazunori, Sugamura, Kazuo, Shibata, Chikashi, Katayose, Yu, Satoh, Kennichi, Tamai, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586677/
https://www.ncbi.nlm.nih.gov/pubmed/34424582
http://dx.doi.org/10.1111/cas.15115
Descripción
Sumario:Cancer stem cells (CSCs) are responsible for therapy resistance and share several properties with normal stem cells. Here, we show that brain‐expressed X‐linked gene 2 (BEX2), which is essential for dormant CSCs in cholangiocarcinoma, is highly expressed in human hepatocellular carcinoma (HCC) lesions compared with the adjacent normal lesions and that in 41 HCC cases the BEX2(high) expression group is correlated with a poor prognosis. BEX2 localizes to Ki67‐negative (nonproliferative) cancer cells in HCC tissues and is highly expressed in the dormant fraction of HCC cell lines. Knockdown of BEX2 attenuates CSC phenotypes, including sphere formation ability and aldefluor activity, and BEX2 overexpression enhances these phenotypes. Moreover, BEX2 knockdown increases cisplatin sensitivity, and BEX2 expression is induced by cisplatin treatment. Taken together, these data suggest that BEX2 induces dormant CSC properties and affects the prognosis of patients with HCC.