MiR-7-5p/KLF4 signaling inhibits stemness and radioresistance in colorectal cancer

Yuanyuan Shang; Zhe Zhu; Yuanyuan Zhang; Fang Ji; Lian Zhu; Mengcheng Liu; Yewei Deng; Guifen Lv; Dan Li; Zhuqing Zhou; Bing Lu; Chuan-Gang Fu

doi:10.1038/s41420-023-01339-8

MiR-7-5p/KLF4 signaling inhibits stemness and radioresistance in colorectal cancer

Cell Death Discov. 2023 Feb 2;9(1):42. doi: 10.1038/s41420-023-01339-8.

Authors

Yuanyuan Shang^#¹, Zhe Zhu^#¹, Yuanyuan Zhang^#¹, Fang Ji¹, Lian Zhu², Mengcheng Liu¹, Yewei Deng¹, Guifen Lv¹, Dan Li¹, Zhuqing Zhou³, Bing Lu⁴, Chuan-Gang Fu⁵

Affiliations

¹ Department of Colorectal Surgery, Department of General Surgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China.
² Department of Radiation Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China.
³ Department of Colorectal Surgery, Department of General Surgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China. zzq2421989@163.com.
⁴ Department of Colorectal Surgery, Department of General Surgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China. 13917955594@163.com.
⁵ Department of Colorectal Surgery, Department of General Surgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China. fugang416@126.com.

^# Contributed equally.

Abstract

Resistance to radiotherapy remains a major unmet clinical obstacle in the treatment of locally advanced rectal cancer. Cancer stem cells (CSCs) are considered to mediate tumor development and radioresistance. However, the role of CSCs in regulating resistance to radiotherapy in colorectal cancer (CRC) remains largely unknown. We established two radioresistant CRC cell lines, HCT116-R and RKO-R, using fractionated irradiation. Analysis using miRNA sequencing and quantitative real-time PCR confirmed lower levels of miR-7-5p in both of the radioresistant cells compared to their parental cells. Subsequently, we validated that miR-7-5p expression was decreased in cancerous tissues from radiotherapy-resistant rectal cancer patients. The Cancer Genome Atlas (TCGA) database analyses revealed that low miR-7-5p expression was significantly correlated with poor prognosis in CRC patients. Overexpression of miR-7-5p led to a rescue of radioresistance and an increase in radiation-induced apoptosis, and attenuated the stem cell-like properties in HCT116-R and RKO-R cells. Conversely, knocking down miR-7-5p in parental HCT116 and RKO cells suppressed the sensitivity to radiation treatment and enhance cancer cell stemness. Stemness-associated transcription factor KLF4 was demonstrated as a target of miR-7-5p. Rescue experiments revealed that miR-7-5p/KLF4 axis could induce radiosensitivity by regulating CSCs in colorectal cancer cells. Furthermore, we used CRC tumor tissues which exhibited resistance to neoadjuvant radiotherapy to establish a patient-derived xenograft (PDX) mouse model. Tail vein injection of magnetic nanoparticles carrying miR-7-5p mimics into the PDX mice significantly inhibited tumor growth with or without irradiation treatment in vivo. Our current studies not only demonstrate an anti-cancer function of miR-7-5p in regulating CSC properties and radiosensitivity in colorectal cancer, but also provide a novel potential strategy for delaying or reverse radiation resistance in preoperative radiotherapy of CRC patients.