Medical Oncology Unit, Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Medical Oncology Unit, Oncology Center, Mansoura University, Mansoura, Egypt.
Breast Dis. 2021;40(2):75-83. doi: 10.3233/BD-201009.
Transforming growth factor-β (TGFβ) has a dual function in breast cancer, having a tumor suppressor activity in early carcinomas while enhancing tumor metastasis in advanced breast carcinoma. Consequently, the prognostic role of TGFβ and its signaling cascade in breast cancer remain unclear.
To investigate the relationship between TβRII expression, clinic-pathological characteristics, and prognostic significance of TβRII expression in clinical stage III breast cancer.
Biopsy from the primary tumor was obtained from 30 newly diagnosed clinical stage III breast cancer patients before receiving any therapy. Expression of TβRII, ER, PR, Her2 and Ki-67 was assessed by immunohistochemistry.
TβRII expression was positive in 66.7% of cases and was significantly associated with advanced nodal stage and distant metastases. After a median follow up of 42.3 months, TβRII was associated with poor disease-free survival and it was an independent factor for predicting the poor outcome for breast cancer patients, especially in node positive tumors, ER/PR positive and Her2-negative tumors.
These findings suggest the usage of therapeutic drugs that target TGFβ in advanced breast cancer patients may be effective. Nevertheless, blockage of the tumor promoting and sparing of the tumor suppressor effect of TGFβ pathway should be taken into consideration. We suggest that these therapies might have more benefit in ER and PR positive tumors.
转化生长因子-β(TGFβ)在乳腺癌中具有双重功能,在早期癌中具有肿瘤抑制活性,而在晚期乳腺癌中则增强肿瘤转移。因此,TGFβ及其信号级联在乳腺癌中的预后作用仍不清楚。
研究 TβRII 表达与临床 III 期乳腺癌临床病理特征及预后的关系。
收集 30 例新诊断的临床 III 期乳腺癌患者在接受任何治疗前的原发肿瘤活检组织。采用免疫组织化学法检测 TβRII、ER、PR、Her2 和 Ki-67 的表达。
TβRII 表达阳性率为 66.7%,与淋巴结转移程度和远处转移显著相关。中位随访 42.3 个月后,TβRII 与无病生存率差相关,是乳腺癌患者不良预后的独立预测因素,尤其是在淋巴结阳性、ER/PR 阳性和 Her2 阴性的肿瘤中。
这些发现提示针对晚期乳腺癌患者 TGFβ 的治疗药物可能有效。然而,应该考虑到阻断 TGFβ 通路的促肿瘤作用并保留其肿瘤抑制作用。我们建议这些治疗方法可能对 ER 和 PR 阳性肿瘤更有益。