A comprehensive overview of metaplastic breast cancer: clinical features and molecular aberrations

被引:114
作者
Reddy, Tejaswini P. [1 ,2 ]
Rosato, Roberto R. [1 ]
Li, Xiaoxian [3 ]
Moulder, Stacy [4 ]
Piwnica-Worms, Helen [4 ]
Chang, Jenny C. [1 ,5 ]
机构
[1] Houston Methodist Res Inst, 6670 Bertner Ave, Houston, TX 77030 USA
[2] Texas A&M Hlth Sci Ctr, Coll Med, 8447 Riverside Pkwy, Bryan, TX 77807 USA
[3] Emory Univ, Sch Med, Winship Canc Inst, 1365 Clifton Rd, Atlanta, GA 30322 USA
[4] Univ Texas MD Anderson Canc Ctr, 1400 Holcombe Blvd, Houston, TX 77030 USA
[5] Weill Cornell Med, Houston Methodist Canc Ctr, OPC 24,6445 Main St, Houston, TX 77030 USA
关键词
Metaplastic breast cancer; PI3K signaling; NOS signaling; Epithelial-to-mesenchymal transition; TO-MESENCHYMAL TRANSITION; CARCINOMA; PATHWAY; EGFR; OVEREXPRESSION; AMPLIFICATION; INHIBITION; EXPRESSION; LANDSCAPE; THERAPY;
D O I
10.1186/s13058-020-01353-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metaplastic breast cancer (MpBC) is an exceedingly rare breast cancer variant that is therapeutically challenging and aggressive. MpBC is defined by the histological presence of at least two cellular types, typically epithelial and mesenchymal components. This variant harbors a triple-negative breast cancer (TNBC) phenotype, yet has a worse prognosis and decreased survival compared to TNBC. There are currently no standardized treatment guidelines specifically for MpBC. However, prior studies have found that MpBC typically has molecular alterations in epithelial-to-mesenchymal transition, amplification of epidermal growth factor receptor, PI3K/Akt signaling, nitric oxide signaling, Wnt/beta-catenin signaling, altered immune response, and cell cycle dysregulation. Some of these molecular alterations have been studied as therapeutic targets, in both the preclinical and clinical setting. This current review discusses the histological organization and cellular origins of MpBC, molecular alterations, the role of radiation therapy, and current clinical trials for MpBC.
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页数:11
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