Li Ruixi, Liu Lulu, Liu Yong, Tang Jiang, Li Jinsong
Yueyang Guangji Hospital, Yueyang, Hunan, People's Republic of China.
Department of Spine Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, People's Republic of China.
Breast Cancer (Dove Med Press). 2024 Sep 9;16:583-593. doi: 10.2147/BCTT.S476083. eCollection 2024.
Protocadherin 9 (PCDH9), a member of the cadherin superfamily of transmembrane proteins, plays a role in cell adhesion and neural development. Recent studies suggest that PCDH9 may function as a tumor suppressor in certain cancers, though its specific role in breast cancer remains unclear.
UALCAN database to retrieve information on PCDH9 expression in breast cancer tissues compared with that in normal tissues. The biological effects of PCDH9 in breast cancer cells were analyzed using the DepMap database. Stable knockdown or overexpression of PCDH9 in breast cancer cell lines and subsequently assessed tumor cell proliferation and migration. Synthetic lethal screening was conducted for breast cancer cells with low PCDH9 expression or deficiency.
In this study, we observed significant downregulation of PCDH9 in breast cancer tissues, with its expression negatively correlated with progression-free survival. Further investigations revealed that decreased PCDH9 expression promotes breast cancer cell proliferation and migration, while overexpression of PCDH9 has the opposite effect. Subsequently, we identified the TAS-102, an approved drug for metastatic colorectal cancer, exhibited selective cytotoxicity against breast cancer cells with low PCDH9 expression.
In summary, our study identified PCDH9 as a tumor suppressor in breast cancer and highlighted TAS-102 as a potential therapeutic option for tumors with low PCDH9 expression or deficiency. The specific interaction between TAS-102 and PCDH9 warrants further exploration, providing deeper insights into its mode of action in treating PCDH9-deficient breast cancer.
原钙黏蛋白9(PCDH9)是跨膜蛋白钙黏蛋白超家族的成员,在细胞黏附和神经发育中发挥作用。最近的研究表明,PCDH9在某些癌症中可能起到肿瘤抑制作用,但其在乳腺癌中的具体作用仍不清楚。
使用UALCAN数据库检索乳腺癌组织与正常组织中PCDH9表达的信息。利用DepMap数据库分析PCDH9在乳腺癌细胞中的生物学效应。在乳腺癌细胞系中稳定敲低或过表达PCDH9,随后评估肿瘤细胞的增殖和迁移。对PCDH9表达低或缺乏的乳腺癌细胞进行合成致死筛选。
在本研究中,我们观察到乳腺癌组织中PCDH9显著下调,其表达与无进展生存期呈负相关。进一步研究表明,PCDH9表达降低促进乳腺癌细胞增殖和迁移,而PCDH9过表达则有相反的效果。随后,我们发现已获批用于转移性结直肠癌的药物TAS-102对PCDH9表达低的乳腺癌细胞具有选择性细胞毒性。
总之,我们的研究确定PCDH9为乳腺癌中的肿瘤抑制因子,并强调TAS-102作为PCDH9表达低或缺乏的肿瘤的潜在治疗选择。TAS-102与PCDH9之间的具体相互作用值得进一步探索,这将为其治疗PCDH9缺陷型乳腺癌的作用方式提供更深入的见解。