Suppr超能文献

Src 家族激酶、HCK 和 FGR 与结直肠癌中的局部炎症和肿瘤进展相关。

Src family kinases, HCK and FGR, associate with local inflammation and tumour progression in colorectal cancer.

机构信息

Academic Unit of Surgery, School of Medicine, University of Glasgow, Royal Infirmary, Glasgow, United Kingdom; Unit of Experimental Therapeutics, Institute of Cancer Sciences, University of Glasgow, Garscube Estate, Glasgow, United Kingdom.

Division of Cancer and Genetics, Cardiff University, Heath Park, Cardiff, United Kingdom.

出版信息

Cell Signal. 2019 Apr;56:15-22. doi: 10.1016/j.cellsig.2019.01.007. Epub 2019 Jan 23.

Abstract

BACKGROUND

In colorectal cancer (CRC), inflammatory responses have been reported to associate with patient survival. However, the specific signalling pathways responsible for regulating inflammatory responses are not clear. Src family kinases (SFKs) impact tumourigenic processes, including inflammation.

METHODS

The relationship between SFK expression, inflammatory responses and cancer specific survival (CSS) in stage I-III CRC patients was assessed using immunohistochemistry on a 272 patient discovery cohort and an extended 822 patient validation cohort.

RESULTS

In the discovery cohort, cytoplasmic FGR associated with improved CSS (P = 0.019), with membrane HCK (p = 0.093) trending towards poorer CSS. In the validation cohort membrane FGR (p = 0.016), membrane HCK (p = 0.019), and cytoplasmic HCK (p = 0.030) all associated with poorer CSS. Both markers also associated with decreased proliferation and cytotoxic T-lymphocytes (all p < 0.05). Furthermore, cytoplasmic HCK was an independent prognostic marker compared to common clinical factors. To assess synergy a combine FGR + HCK score was assessed. The membrane FGR + HCK score strengthened associations with poor prognosis (p = 0.006), decreased proliferation (p < 0.001) and cytotoxic T-lymphocytes (p < 0.001).

CONCLUSIONS

SFKs associate with prognosis and the local inflammatory response in patients with stage I-III CRC. Active membrane FGR and HCK work in parallel to promote tumour progression and down-regulation of the local inflammatory lymphocytic response.

摘要

背景

在结直肠癌(CRC)中,已经报道炎症反应与患者生存相关。然而,负责调节炎症反应的特定信号通路尚不清楚。Src 家族激酶(SFKs)影响肿瘤发生过程,包括炎症。

方法

使用免疫组织化学方法在 272 名患者的发现队列和 822 名扩展患者验证队列中评估 SFK 表达、炎症反应与 I-III 期 CRC 患者的癌症特异性生存(CSS)之间的关系。

结果

在发现队列中,细胞质 FGR 与 CSS 改善相关(P=0.019),而膜 HCK(p=0.093)则趋势较差。在验证队列中,膜 FGR(p=0.016)、膜 HCK(p=0.019)和细胞质 HCK(p=0.030)均与 CSS 较差相关。这两种标志物也与增殖减少和细胞毒性 T 淋巴细胞减少相关(均 P<0.05)。此外,细胞质 HCK 与常见临床因素相比是独立的预后标志物。为了评估协同作用,评估了联合 FGR+HCK 评分。膜 FGR+HCK 评分与预后不良(p=0.006)、增殖减少(p<0.001)和细胞毒性 T 淋巴细胞减少(p<0.001)的相关性增强。

结论

SFKs 与 I-III 期 CRC 患者的预后和局部炎症反应相关。活跃的膜 FGR 和 HCK 平行作用,促进肿瘤进展和下调局部炎症性淋巴细胞反应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验