FBL promotes cancer cell resistance to DNA damage and BRCA1 transcription via YBX1

Author:

Sun Xiaorui1ORCID,Gao Congwen1ORCID,Xu Xin1ORCID,Li Mengyuan1,Zhao Xinhua1,Wang Yanan2ORCID,Wang Yun2,Zhang Shun2ORCID,Yan Zhenzhen1ORCID,Liu Xiuhua1ORCID,Wu Chen13ORCID

Affiliation:

1. College of Life Sciences Hebei University Baoding China

2. Affiliated Hospital of Hebei University Baoding China

3. The Key Laboratory of Zoological Systematics and Application Hebei University Baoding China

Abstract

AbstractFibrillarin (FBL) is a highly conserved nucleolar methyltransferase responsible for methylation of ribosomal RNA and proteins. Here, we reveal a role for FBL in DNA damage response and its impact on cancer proliferation and sensitivity to DNA‐damaging agents. FBL is highly expressed in various cancers and correlates with poor survival outcomes in cancer patients. Knockdown of FBL sensitizes tumor cells and xenografts to DNA crosslinking agents, and leads to homologous recombination‐mediated DNA repair defects. We identify Y‐box‐binding protein‐1 (YBX1) as a key interacting partner of FBL, and FBL increases the nuclear accumulation of YBX1 in response to DNA damage. We show that FBL promotes the expression of BRCA1 by increasing the binding of YBX1 to the BRCA1 promoter. Our study sheds light on the regulatory mechanism of FBL in tumorigenesis and DNA damage response, providing potential therapeutic targets to overcome chemoresistance in cancer.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hebei Province

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

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