High-fat diet induced cyclophilin B enhances STAT3/lncRNA-PVT1 feedforward loop and promotes growth and metastasis in colorectal cancer

• Published in: Cell death & disease Vol. 13; no. 10; pp. 883 - 17
• Main Authors: Guo, Hanqing, Zhuang, Kun, Ding, Ning, Hua, Rui, Tang, Hailing, Wu, Yue, Yuan, Zuyi, Li, Ting, He, Shuixiang
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.10.2022; Springer Nature B.V; Nature Publishing Group
• Subjects: 13/1; 13/109; 13/2; 13/21; 13/31; 13/51; 13/89; 13/95; 14/105; 14/19; 14/5; 42/70; 631/337/384/2568; 631/67/1504/1885; 64/60; Animals; Antibodies; Biochemistry; Biomedical and Life Sciences; Body mass index; Carcinogenesis; Cell Biology; Cell Culture; Cholesterol; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - genetics; Colorectal Neoplasms - pathology; Diet, High-Fat; High fat diet; Immunology; Inflammation; Interleukin 6; Interleukin-6 - metabolism; Life Sciences; Malignancy; Metastases; Metastasis; Mice; Non-coding RNA; Nuclear transport; Phosphorylation; RNA, Long Noncoding - genetics; RNA, Long Noncoding - metabolism; Stat3 protein; STAT3 Transcription Factor - genetics; STAT3 Transcription Factor - metabolism; Transcription
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-022-05328-0

High-fat diet (HFD) has been implicated to promote colorectal cancer (CRC). Recently, oncogene Cyclophilin B (CypB) is reported to be induced by cholesterol. However, the role of CypB in CRC carcinogenesis and metastasis associated with HFD remains unknown. In the present study, we showed that HFD-induced CypB enhances proliferation and metastasis through an inflammation-driven circuit, including Signal Transducer and Activator of Transcription 3 (STAT3)-triggered transcription of lncRNA-PVT1, and its binding with CypB that promotes activation of STAT3. CypB was found to be upregulated in CRC, which was correlated with elevated body mass index and poor prognosis. HFD induced CypB expression and proinflammatory cytokines in colon of mice. Besides, CypB restoration facilitated growth, invasion and metastasis in CRC cells both in vitro and in vivo. Moreover, RIP sequencing data identified lncRNA-PVT1 as a functional binding partner of CypB. Mechanistically, PVT1 increased the phosphorylation and nuclear translocation of STAT3 in response to IL-6, through directly interaction with CypB, which impedes the binding of Suppressors Of Cytokine Signalling 3 (SOCS3) to STAT3. Furthermore, STAT3 in turn activated PVT1 transcription through binding to its promoter, forming a regulatory loop. Finally, this CypB/STAT3/PVT1 axis was verified in TCGA datasets and CRC tissue arrays. Our data revealed that CypB linked HFD and CRC malignancy by enhancing the CypB/STAT3/PVT1 feedforward axis and activation of STAT3.