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脑转移瘤中 CXCL12、CXCR4 和 CXCR7 的表达。

CXCL12, CXCR4 and CXCR7 expression in brain metastases.

机构信息

Department of Neurology, Fondazione IRCCS Istituto Neurologico C. Besta, Via Celoria 11, Milan, Italy.

出版信息

Cancer Biol Ther. 2009 Sep;8(17):1608-14. doi: 10.4161/cbt.8.17.9202. Epub 2009 Sep 6.

Abstract

Brain metastases occur in about 25% of patients who die of cancer. The most common sources of brain metastases in adults are lung, breast, kidney, colorectal cancer and melanoma. The chemokine/receptor system CXCL12/CXCR4 plays a key role in multiple biological functions; among these, homing of neoplastic cells from the primary site to the target and metastasis progression. Recently, an alternative CXCL12 receptor CXCR7 has been discovered. The aim of our study was to investigate the expression of CXCL12 and its receptors CXCR4 and CXCR7 by immunohistochemistry in 56 patients with metastatic brain disease from different non-CNS primary tumors and evaluate their prognostic relevance as well as that of other patient/treatment-related features on patient survival. CXCL12 showed an expression in tumor cells and in tumor vessels; CXCR7 was expressed by tumor and endothelial cells (both within the tumor and in the adjacent brain tissue), while CXCR4 showed a positivity in all samples with a nuclear pattern. Among the investigated immunohistochemical parameters, only CXCL12 expression in tumor endothelial cells showed a statistically significant correlation with shorter survival (p = 0.04 log-rank), perhaps identifying more aggressive tumors. Thus, this is the first study evaluating at the same time the expression of CXCL12 and its two receptors in a cohort of brain metastases.

摘要

脑转移发生在约 25%死于癌症的患者中。成年人脑转移最常见的来源是肺癌、乳腺癌、肾癌、结直肠癌和黑色素瘤。趋化因子/受体系统 CXCL12/CXCR4 在多种生物学功能中起着关键作用;其中包括肿瘤细胞从原发部位向靶器官的归巢和转移进展。最近,发现了一种替代的 CXCL12 受体 CXCR7。我们的研究目的是通过免疫组织化学检测来自不同非中枢神经系统原发性肿瘤的 56 例转移性脑疾病患者中 CXCL12 及其受体 CXCR4 和 CXCR7 的表达,并评估它们的预后相关性以及其他与患者/治疗相关的特征对患者生存的影响。CXCL12 在肿瘤细胞和肿瘤血管中表达;CXCR7 由肿瘤细胞和内皮细胞(肿瘤内和相邻脑组织内)表达,而 CXCR4 在所有样本中均呈阳性,呈核模式。在所研究的免疫组织化学参数中,只有肿瘤内皮细胞中 CXCL12 的表达与较短的生存时间呈统计学显著相关性(p = 0.04 log-rank),这可能表明肿瘤更具侵袭性。因此,这是首次在脑转移瘤队列中同时评估 CXCL12 及其两种受体表达的研究。

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