RSRC2 Expression Inhibits Malignant Progression of Triple-Negative Breast Cancer by Transcriptionally Regulating SCIN Expression

• Published in: Cancers Vol. 16; no. 1; p. 15
• Main Authors: Zhao, Nan, Ni, Chunsheng, Fan, Shuai, Che, Na, Li, Yanlei, Wang, Song, Li, Yongli, Dong, Xueyi, Guo, Yuhong, Zhao, Xiulan, Liu, Tieju
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 19.12.2023; MDPI
• Subjects: Analysis; Antibodies; Apoptosis; Bioinformatics; Breast cancer; Cancer patients; Cancer therapies; Cell adhesion; Cell growth; Cell migration; Cell proliferation; Chemotherapy; Development and progression; Esophageal cancer; Gastric cancer; Genetic transcription; Health aspects; Liver cancer; Metastases; Metastasis; Plasmids; Prognosis; Prostate cancer; Proteins; RSRC2; SCIN; Statistical analysis; Transcription; transcriptional regulation; Transcriptomes; triple-negative breast cancer; Tumor suppressor genes; Tumors; China; United States > US; triple-negative breast cancer; RSRC2; SCIN; transcriptional regulation
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers16010015

Triple-negative breast cancer (TNBC) has a shorter survival time and higher mortality rate than other molecular subtypes. RSRC2 is a newly discovered tumor suppressor gene. However, the potential functional mechanism of RSRC2 in TNBC remains unknown so far. Multiple bioinformatics databases were used. A Human Transcriptome Array 2.0 analysis, ChIP-seq analysis, ChIP-qPCR, RT-qPCR, Western blot, cell function assays in vitro and a metastatic mouse model in vivo were performed to demonstrate the role of RSRC2 in TNBC. Through the analysis of various databases, RSRC2 expression was the lowest in TNBC tissues compared to other molecular subtypes. The low expression of RSRC2 was associated with a worse prognosis for patients with breast cancer. The transcriptome array, ChIP-seq and bioinformatics analysis identified that GRHL2 and SCIN might have a close relationship with RSRC2. The functional bioinformatics enrichment analysis and functional cell experiments showed that RSRC2 was involved in cell adhesion, cell proliferation, cell migration and invasion. Furthermore, RSRC2 expression suppressed SCIN expression but not GRHL2 expression. SCIN re-expression in the RSRC2 overexpression cells or SCIN knockdown in the RSRC2 knockdown cells reversed the cellular function caused by RSRC2. Mechanistically, RSRC2 transcriptionally inhibited SCIN expression. In summary, our study reveals that RSRC2 acts as a tumor suppressor in TNBC development and progression through negatively regulating SCIN-mediated cell function, thus providing a potential target for TNBC treatment.