Genome-wide CRISPR/Cas9 screening identifies CARHSP1 responsible for radiation resistance in glioblastoma.

Abstract

Glioblastomas (GBM) is the most common primary malignant brain tumor, and radiotherapy plays a critical role in its therapeutic management. Unfortunately, the development of radioresistance is universal. Here, we identified calcium-regulated heat-stable protein 1 (CARHSP1) as a critical driver for radioresistance utilizing genome-wide CRISPR activation screening. This is a protein with a cold-shock domain (CSD)-containing that is highly similar to cold-shock proteins. CARHSP1 mRNA level was upregulated in irradiation-resistant GBM cells and knockdown of CARHSP1 sensitized GBM cells to radiotherapy. The high expression of CARHSP1 upon radiation might mediate radioresistance by activating the inflammatory signaling pathway. More importantly, patients with high levels of CARHSP1 had poorer survival when treated with radiotherapy. Collectively, our findings suggested that targeting the CARHSP1/TNF-α inflammatory signaling activation induced by radiotherapy might directly affect radioresistance and present an attractive therapeutic target for GBM, particularly for patients with high levels of CARHSP1.

• Authors: Guo-Dong Zhu, Jing Yu, Zheng-Yu Sun, Yan Chen, Hong-Mei Zheng, Mei-Lan Lin, Shi Ou-Yang, Guo-Long Liu, Jie-Wen Zhang, Feng-Min Shao
• Journal: Cell death & disease (Cell Death Dis) Vol. 12 Issue 8 Pg. 724 (07 21 2021) ISSN: 2041-4889 [Electronic] England
• PMID: 34290231 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2021. The Author(s).

Chemical References

• CARHSP1 protein, human
• DNA-Binding Proteins
• Phosphoproteins
• RNA, Messenger
• Transcription Factors
• Tumor Necrosis Factor-alpha
• CRISPR-Associated Protein 9

Topics

• Brain Neoplasms (genetics, pathology, radiotherapy)
• CRISPR-Associated Protein 9 (metabolism)
• CRISPR-Cas Systems (genetics)
• Cell Line, Tumor
• DNA-Binding Proteins (genetics, metabolism)
• Drug Resistance, Neoplasm (genetics)
• Gene Expression Regulation, Neoplastic
• Genome, Human
• Glioblastoma (genetics, pathology, radiotherapy)
• Humans
• Phosphoproteins (genetics, metabolism)
• RNA, Messenger (genetics, metabolism)
• Radiation Tolerance (genetics)
• Transcription Factors (genetics, metabolism)
• Tumor Necrosis Factor-alpha (metabolism)
• Up-Regulation (genetics)