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转化生长因子β1和转化生长因子β3在人类乳腺癌中的预后意义

Prognostic significance of TGF beta 1 and TGF beta 3 in human breast carcinoma.

作者信息

Ghellal A, Li C, Hayes M, Byrne G, Bundred N, Kumar S

机构信息

Manchester University and Christie Hospital, Manchester, M13 9PT, U.K.

出版信息

Anticancer Res. 2000 Nov-Dec;20(6B):4413-8.

Abstract

Transforming growth factor beta s (TGF beta s) are multifunctional growth factors which show differential expression both temporally and spatially and exert pleiotropic effects during carcinogenesis. Although all three mammalian isoforms of TGF beta share considerable sequence similarity, they appear to have distinct functions in health and disease, such as embryogenesis, wound healing and tumourigenesis. Much of our knowledge about the relationship between TGF beta s and breast cancer is based on publications on TGF beta 1 but the role of TGF beta 3 in the progression of breast cancer has not been well documented. In the present study, the expression of TGF beta 1 and TGF beta 3 was assessed by immunohistochemistry. Of the 153 invasive breast cancer tissues, TGF beta 1 was expressed strongly in 25 and moderately in 98 cases. The immunoreactivity of TGF beta 3 was comparable with TGF beta 1, which was expressed strongly in 21 and moderately in 104 cases. The two isoforms were coexpressed in 111 (72.5%) tumours and were absent in 16 cases (10%). Immunostaining for TGFb3 but not TGF beta 1 was inversely correlated with overall survival (p = 0.0204). When combined with lymph node involvement, TGFb3 became an even more significant prognostic factor for overall survival (p = 0.0003), i.e. patients with node metastasis and positive TGFb3 expression had a worse prognosis: the risk of death for these patients was thirteen-fold greater than those who had no node involvement. The fact that it has been reported previously that high TGF beta 3 plasma levels in patients with untreated early stage breast cancer were correlated with subsequent lymph node metastasis and it was observed in the present study too, that TGF beta 3 expression in breast tumours was an independent predictor of overall survival, led us to suggest that the simultaneous measurement of TGF beta 3 in plasma and its expression in resected tumour tissues in the same cohort of patients may prove to be an important parameter in assessing tumour progression.

摘要

转化生长因子β(TGF-β)是多功能生长因子,在时间和空间上呈现差异表达,并在肿瘤发生过程中发挥多效性作用。尽管TGF-β的三种哺乳动物同工型具有相当大的序列相似性,但它们在健康和疾病(如胚胎发生、伤口愈合和肿瘤发生)中似乎具有不同的功能。我们关于TGF-β与乳腺癌之间关系的许多知识都基于关于TGF-β1的出版物,但TGF-β3在乳腺癌进展中的作用尚未得到充分记录。在本研究中,通过免疫组织化学评估了TGF-β1和TGF-β3的表达。在153例浸润性乳腺癌组织中,25例TGF-β1强表达,98例中度表达。TGF-β3的免疫反应性与TGF-β1相当,21例强表达,104例中度表达。这两种同工型在111例(72.5%)肿瘤中共同表达,16例(10%)中不存在。TGF-β3而非TGF-β1的免疫染色与总生存期呈负相关(p = 0.0204)。当与淋巴结受累相结合时,TGF-β3成为总生存期更显著的预后因素(p = 0.0003),即有淋巴结转移且TGF-β3表达阳性的患者预后更差:这些患者的死亡风险比无淋巴结受累的患者高13倍。先前有报道称,未经治疗的早期乳腺癌患者血浆中高TGF-β3水平与随后的淋巴结转移相关,本研究也观察到,乳腺肿瘤中TGF-β3的表达是总生存期的独立预测因子,这使我们认为,在同一组患者中同时测量血浆中的TGF-β3及其在切除肿瘤组织中的表达可能是评估肿瘤进展的一个重要参数。

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