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GRK3 过表达促进肿瘤增殖,预示结直肠癌预后不良。

Overexpression of GRK3, Promoting Tumor Proliferation, Is Predictive of Poor Prognosis in Colon Cancer.

机构信息

Department of Anal-Colorectal Surgery, General Hospital of Ningxia Medical University, 804 South Shengli Road, Yinchuan 750004, China.

Department of Ultrasound, General Hospital of Ningxia Medical University, 804 South Shengli Road, Yinchuan 750004, China.

出版信息

Dis Markers. 2017;2017:1202710. doi: 10.1155/2017/1202710. Epub 2017 Dec 28.

Abstract

Deregulation of G protein-coupled receptor kinase 3 (GRK3), which belongs to a subfamily of kinases called GRKs, acts as a promoter mechanism in some cancer types. Our study found that GRK3 was significantly overexpressed in 162 pairs of colon cancer tissues than in the matched noncancerous mucosa ( < 0.01). Based on immunohistochemistry staining of TMAs, GRK3 was dramatically stained positive in primary colon cancer (130/180, 72.22%), whereas it was detected minimally or negative in paired normal mucosa specimens (50/180, 27.78%). Overexpression of GRK3 was closely correlated with AJCC stage ( = 0.001), depth of tumor invasion ( < 0.001), lymph node involvement ( = 0.004), distant metastasis ( = 0.016), and histologic differentiation ( = 0.004). Overexpression of GRK3 is an independent prognostic indicator that correlates with poor survival in colon cancer patients. Consistent with this, downregulation of GRK3 exhibited decreased cell growth index, reduction in colony formation ability, elevated cell apoptosis rate, and impaired colon tumorigenicity in a xenograft model. Hence, a specific overexpression of GRK3 was observed in colon cancer, GRK3 potentially contributing to progression by mediating cancer cell proliferation and functions as a poor prognostic indicator in colon cancer and potentially represent a novel therapeutic target for the disease.

摘要

G 蛋白偶联受体激酶 3(GRK3)的失调属于激酶家族的一个亚家族,在某些癌症类型中作为促进机制起作用。我们的研究发现,GRK3 在 162 对结肠癌组织中的表达明显高于配对的非癌性黏膜(<0.01)。基于 TMAs 的免疫组化染色,GRK3 在原发性结肠癌中明显呈阳性染色(130/180,72.22%),而在配对的正常黏膜标本中则检测到最小或阴性(50/180,27.78%)。GRK3 的过表达与 AJCC 分期密切相关(=0.001),肿瘤侵袭深度(<0.001),淋巴结受累(=0.004),远处转移(=0.016)和组织学分化(=0.004)。GRK3 的过表达是结肠癌患者独立的预后指标,与不良生存相关。与此一致的是,在异种移植模型中下调 GRK3 可降低细胞生长指数,减少集落形成能力,提高细胞凋亡率并损害结肠肿瘤发生能力。因此,在结肠癌中观察到 GRK3 的特异性过表达,GRK3 通过介导癌细胞增殖而潜在地促进疾病进展,并且作为结肠癌的不良预后指标,并可能代表该疾病的新型治疗靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449a/5763208/fffd5f8f8601/DM2017-1202710.001.jpg

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