Nahta Rita, Esteva Francisco J
Department of Breast Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030-4009, USA.
Cancer Lett. 2006 Feb 8;232(2):123-38. doi: 10.1016/j.canlet.2005.01.041.
HER-2 is overexpressed in 20-25% of invasive breast cancers and is associated with an aggressive tumor phenotype and reduced survival rate. The HER-2 status of a tumor is the critical determinant of response to the HER-2-targeted antibody Herceptin. Thus, accurate assessment of HER-2 expression levels is essential for identifying breast cancer patients who will benefit from HER-2-targeted therapy. Herceptin combined with chemotherapy increases response rates, time to disease progression, and survival. However, the majority of cancers that initially respond to Herceptin begin to progress again within 1 year. This review describes mechanisms by which Herceptin inhibits cell growth in breast cancers that overexpress HER-2 and highlights possible mechanisms contributing to Herceptin resistance.
HER-2在20%-25%的浸润性乳腺癌中过度表达,与侵袭性肿瘤表型和较低的生存率相关。肿瘤的HER-2状态是对HER-2靶向抗体赫赛汀反应的关键决定因素。因此,准确评估HER-2表达水平对于识别将从HER-2靶向治疗中获益的乳腺癌患者至关重要。赫赛汀联合化疗可提高缓解率、疾病进展时间和生存率。然而,大多数最初对赫赛汀有反应的癌症在1年内会再次进展。这篇综述描述了赫赛汀抑制HER-2过表达的乳腺癌细胞生长的机制,并强调了导致赫赛汀耐药的可能机制。