Li Xingzhi, Liang Ziji, Pan Jiexin, Zhang Meng, Liu Jinli, Hu Rong, Liao Caiyan
Department of Urology, The Second Affiliated Hospital of The Chinese University of HongKong/Longgang District People's Hospital of Shenzhen, Shenzhen, 518172, Guangdong, China.
Warshel Institute for Computational Biology, The Chinese University of Hong Kong, Longgang District, Shenzhen, 518172, Guangdong, China.
BMC Cancer. 2024 Mar 11;24(1):328. doi: 10.1186/s12885-024-12061-8.
The sialic acid binding Ig like lectin 15 (Siglec-15) was previously identified as tumor immune suppressor gene in some human cancers with elusive molecular mechanism to be elucidated. The continuous focus on both clinical and basic biology of bladder cancer leads us to characterize aberrant abundance of BACH1-IT2 associating with stabilization of Siglec-15, which eventually contributes to local immune suppressive microenvironment and therefore tumor advance. This effect was evidently mediated by miR-4786-5p. BACH1-IT2 functions in this scenario as microRNA sponge, and competitively conceals miR-4786 and up-regulates cancer cell surface Siglec-15. The BACH1-IT2-miR-4786-Siglec-15 axis significantly influences activation of immune cell co-culture. In summary, our data highlights the critical involvements of BACH1-IT2 and miR-4786 in immune evasion in bladder cancer, which hints the potential for both therapeutic and prognostic exploitation.
唾液酸结合免疫球蛋白样凝集素15(Siglec-15)先前在一些人类癌症中被鉴定为肿瘤免疫抑制基因,但其分子机制尚不清楚。对膀胱癌临床和基础生物学的持续关注使我们对与Siglec-15稳定相关的BACH1-IT2异常丰度进行了表征,这最终导致局部免疫抑制微环境并促进肿瘤进展。这种效应显然是由miR-4786-5p介导的。在这种情况下,BACH1-IT2作为微小RNA海绵发挥作用,竞争性地隐藏miR-4786并上调癌细胞表面的Siglec-15。BACH1-IT2-miR-4786-Siglec-15轴显著影响免疫细胞共培养的激活。总之,我们的数据突出了BACH1-IT2和miR-4786在膀胱癌免疫逃逸中的关键作用,这提示了其在治疗和预后应用方面的潜力。