Sugita Bruna M, Rodriguez Yara, Fonseca Aline S, Nunes Souza Emanuelle, Kallakury Bhaskar, Cavalli Iglenir J, Ribeiro Enilze M S F, Aneja Ritu, Cavalli Luciane R
Research Institute Pele Pequeno Príncipe, Faculdades Pequeno Príncipe Curitiba, Curitiba 80250-060, Brazil.
Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20007, USA.
Cancers (Basel). 2022 Apr 26;14(9):2156. doi: 10.3390/cancers14092156.
MiR-150-5p is frequently deregulated in cancer, with expression and mode of action varying according to the tumor type. Here, we investigated the expression levels and role of miR-150-5p in the aggressive breast cancer subtype triple-negative breast cancer (TNBC). MiR-150-5p expression levels were analyzed in tissue samples from 113 patients with invasive breast cancer (56 TNBC and 57 non-TNBC) and 41 adjacent non-tumor tissues (ANT). Overexpression of miR-150-5p was observed in tumor tissues compared with ANT tissues and in TNBC compared with non-TNBC tissues. MiR-150-5p expression levels were significantly associated with high tumor grades and the Caucasian ethnicity. Interestingly, high miR-150-5p levels were associated with prolonged overall survival. Manipulation of miR-150-5p expression in TNBC cells modulated cell proliferation, clonogenicity, migration, and drug resistance. Manipulation of miR-150-5p expression also resulted in altered expression of its mRNA targets, including epithelial-to-mesenchymal transition markers, , and members of the SRC pathway. These findings suggest that miR-150-5p is overexpressed in TNBC and contributes to the aggressiveness of TNBC cells in vitro.
MiR-150-5p在癌症中常常失调,其表达和作用模式因肿瘤类型而异。在此,我们研究了miR-150-5p在侵袭性乳腺癌亚型三阴性乳腺癌(TNBC)中的表达水平及作用。分析了113例浸润性乳腺癌患者(56例TNBC和57例非TNBC)以及41例癌旁非肿瘤组织(ANT)的组织样本中miR-150-5p的表达水平。与ANT组织相比,在肿瘤组织中观察到miR-150-5p过表达;与非TNBC组织相比,在TNBC中也观察到miR-150-5p过表达。miR-150-5p表达水平与高肿瘤分级及白种人种族显著相关。有趣的是,高miR-150-5p水平与总体生存期延长相关。在TNBC细胞中调控miR-150-5p表达可调节细胞增殖、克隆形成能力、迁移及耐药性。调控miR-150-5p表达还导致其mRNA靶标的表达改变;这些靶标包括上皮-间质转化标志物以及SRC途径的成员。这些发现表明,miR-150-5p在TNBC中过表达,并在体外促进TNBC细胞的侵袭性。