Zhou Jie, Wu Lvying, Xu Pengyan, Li Yue, Ji Zhiliang, Kang Xinmei
Department of Oncology, Xiang'an Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiamen, China.
Front Oncol. 2022 Mar 11;12:836126. doi: 10.3389/fonc.2022.836126. eCollection 2022.
Recurrent metastasis is a major fatal cause of breast cancer. Regretfully, the driving force and the molecular beneath have not been fully illustrated yet. In this study, a cohort of breast cancer patients with locoregional metastasis was recruited. For them, we collected the matched samples of the primary tumor and metastatic tumor, and then we determined the mutation profiles with whole-exome sequencing (WES). On basis of the profiles, we identified a list of deleterious variants in eight susceptible genes. Of them, filamin A (FLNA) was considered a potential driver gene of metastasis, and its low expression could enhance 5 years' relapse survival rate by 15%. To prove the finding, we constructed a stable FLNA knockout tumor cell line, which manifested that the cell abilities of proliferation, migration, and invasion were significantly weakened in response to the gene knockout. Subsequently, xenograft mouse experiments further proved that FLNA knockout could inhibit local or distal metastasis. Putting all the results together, we consolidated that FLNA could be a potential driver gene to metastasis of breast cancer, in particular triple-negative breast cancer. Additional experiments also suggested that FLNA might intervene in metastasis the regulation of MMP-1 expression. In summary, this study demonstrates that FLNA may play as a positive regulator in cancer proliferation and recurrence. It provides new insight into breast cancer metastasis and suggests a potential new therapeutic target for breast cancer therapy.
复发性转移是乳腺癌的主要致死原因。遗憾的是,其驱动因素及背后的分子机制尚未完全阐明。在本研究中,招募了一组发生局部区域转移的乳腺癌患者。针对这些患者,我们收集了原发性肿瘤和转移瘤的配对样本,然后通过全外显子组测序(WES)确定突变谱。基于这些谱,我们在八个易感基因中鉴定出一系列有害变异。其中,细丝蛋白A(FLNA)被认为是转移的潜在驱动基因,其低表达可使5年复发生存率提高15%。为了验证这一发现,我们构建了一个稳定的FLNA敲除肿瘤细胞系,结果表明,基因敲除后细胞的增殖、迁移和侵袭能力显著减弱。随后,异种移植小鼠实验进一步证明FLNA敲除可抑制局部或远处转移。综合所有结果,我们证实FLNA可能是乳腺癌尤其是三阴性乳腺癌转移的潜在驱动基因。额外的实验还表明,FLNA可能通过干预基质金属蛋白酶-1(MMP-1)表达的调控来影响转移。总之,本研究表明FLNA可能在癌症增殖和复发中起正调控作用。它为乳腺癌转移提供了新的见解,并为乳腺癌治疗提出了一个潜在的新治疗靶点。