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趋化因子受体 CXCR4 和 CXCR7 对肾上腺皮质癌临床结局的影响。

Impact of the Chemokine Receptors CXCR4 and CXCR7 on Clinical Outcome in Adrenocortical Carcinoma.

机构信息

Division of Endocrinology and Diabetes, Department of Medicine I, University Hospital of Wuerzburg, University of Wuerzburg, Wuerzburg, Germany.

Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom.

出版信息

Front Endocrinol (Lausanne). 2020 Nov 13;11:597878. doi: 10.3389/fendo.2020.597878. eCollection 2020.

Abstract

Chemokine receptors have a negative impact on tumor progression in several human cancers and have therefore been of interest for molecular imaging and targeted therapy. However, their clinical and prognostic significance in adrenocortical carcinoma (ACC) is unknown. The aim of this study was to evaluate the chemokine receptor profile in ACC and to analyse its association with clinicopathological characteristics and clinical outcome. A chemokine receptor profile was initially evaluated by quantitative PCR in 4 normal adrenals, 18 ACC samples and human ACC cell line NCI-H295. High expression of CXCR4 and CXCR7 in both healthy and malignant adrenal tissue and ACC cells was confirmed. In the next step, we analyzed the expression and cellular localization of CXCR4 and CXCR7 in ACC by immunohistochemistry in 187 and 84 samples, respectively. These results were correlated with clinicopathological parameters and survival outcome. We detected strong membrane expression of CXCR4 and CXCR7 in 50% of ACC samples. Strong cytoplasmic CXCR4 staining was more frequent among samples derived from metastases compared to primaries (0.01) and local recurrences (0.04). CXCR4 membrane staining positively correlated with proliferation index Ki67 (r=0.17, 0.028). CXCR7 membrane staining negatively correlated with Ki67 (r=-0.254, 0.03) but positively with tumor size (r=0.3, 0.02). No differences in progression-free or overall survival were observed between patients with strong and weak staining intensities for CXCR4 or CXCR7. Taken together, high expression of CXCR4 and CXCR7 in both local tumors and metastases suggests that some ACC patients might benefit from CXCR4/CXCR7-targeted therapy.

摘要

趋化因子受体对几种人类癌症的肿瘤进展有负面影响,因此引起了人们对分子成像和靶向治疗的兴趣。然而,它们在肾上腺皮质癌(ACC)中的临床和预后意义尚不清楚。本研究旨在评估 ACC 中的趋化因子受体谱,并分析其与临床病理特征和临床结果的关系。我们首先通过定量 PCR 评估了 4 个正常肾上腺、18 个 ACC 样本和人 ACC 细胞系 NCI-H295 中的趋化因子受体谱。证实了 CXCR4 和 CXCR7 在健康和恶性肾上腺组织以及 ACC 细胞中的高表达。在下一步中,我们通过免疫组织化学分析了 187 个和 84 个样本中 CXCR4 和 CXCR7 的表达和细胞定位。这些结果与临床病理参数和生存结果相关。我们检测到 50%的 ACC 样本中存在 CXCR4 和 CXCR7 的强膜表达。与原发肿瘤(0.01)和局部复发(0.04)相比,转移来源的样本中 CXCR4 细胞质染色较强。CXCR4 膜染色与增殖指数 Ki67 呈正相关(r=0.17,0.028)。CXCR7 膜染色与 Ki67 呈负相关(r=-0.254,0.03),但与肿瘤大小呈正相关(r=0.3,0.02)。CXCR4 或 CXCR7 染色强度强和弱的患者在无进展生存期或总生存期方面没有差异。总之,局部肿瘤和转移瘤中 CXCR4 和 CXCR7 的高表达表明,一些 ACC 患者可能受益于 CXCR4/CXCR7 靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f907/7691376/bd6bd217b96a/fendo-11-597878-g001.jpg

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