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Squamous cell carcinoma related oncogene regulates angiogenesis through vascular endothelial growth factor-A.

机译:鳞状细胞癌相关癌基因通过血管内皮生长因子-A调节血管生成。

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BACKGROUND: Squamous cell carcinoma related oncogene expression (SCCRO) correlates with vascular endothelial growth factor-A expression. This data is validated in human lung tumors and provides a putative pathway for angiogenesis in a subset of squamous cell carcinomas. Squamous cell carcinoma related oncogene is a novel oncogene identified by positional cloning of a recurrent amplification at 3q26.3. It is over-expressed in 39.8% of lung, head and neck, cervical, and ovarian carcinomas. SCCRO imparts an aggressive phenotype to affected cancers, which may be related to increased angiogenesis due to SCCRO expression. Our previous work has demonstrated a link between SCCRO and vascular endothelial growth factor-A (VEGF-A) expression in vitro, suggesting a mechanism for SCCRO-induced angiogenesis. The present study aims to confirm and validate this link between SCCRO and VEGF-A expression in an ex vivo human tumor cohort. METHODS: Fresh tissue was collected at Memorial Sloan-Kettering Cancer Center from 34 patients undergoing primary resection of lung squamous cell carcinomas. RNA was extracted from this tissue, reverse-transcribed, and real-time polymerase chain reaction (RT-PCR) was carried out using a BioRad iQ iCycler with SYBR green fluorophore. Microvessel counting was performed on the tumor specimens using CD34 immunohistochemistry. RESULTS: The expression of both SCCRO and VEGF-A mRNA varies widely in both tumor and normal tissue. SCCRO and VEGF-A co-expression was significantly correlated (R(2) = 0.63; P < 0.032). Microvessel counts were not associated with expression of SCCRO or VEGF-A and failed to significantly predict survival. VEGF-A expression in this patient group is a predictor of overall survival (P < 0.032). CONCLUSIONS: VEGF-A expression correlates with SCCRO expression in these primary human lung squamous cell carcinomas and is a predictor of clinical behavior. This data supports the association of SCRRO and VEGF-A in the induction of angiogenesis.
机译:背景:鳞状细胞癌相关癌基因表达(SCCRO)与血管内皮生长因子-A表达相关。该数据在人肺肿瘤中得到验证,并为鳞状细胞癌的子集提供了血管生成的假定途径。鳞状细胞癌相关致癌基因是一种通过在3q26.3位置重复扩增的位置克隆而鉴定的新型致癌基因。在39.8%的肺癌,头颈癌,宫颈癌和卵巢癌中过表达。 SCCRO将侵袭性表型赋予受影响的癌症,这可能与SCCRO表达导致的血管生成增加有关。我们以前的工作已经证明了SCCRO和体外血管内皮生长因子-A(VEGF-A)表达之间的联系,暗示了SCCRO诱导的血管生成的机制。本研究旨在证实和验证体外人肿瘤队列中SCCRO和VEGF-A表达之间的这种联系。方法:从纪念斯隆-凯特琳癌症中心收集34例行肺鳞状细胞癌初次切除的患者的新鲜组织。从该组织中提取RNA,逆转录,然后使用带有SYBR绿色荧光团的BioRad iQ iCycler进行实时聚合酶链反应(RT-PCR)。使用CD34免疫组织化学对肿瘤标本进行微血管计数。结果:在肿瘤组织和正常组织中,SCCRO和VEGF-A mRNA的表达差异很大。 SCCRO和VEGF-A共表达显着相关(R(2)= 0.63; P <0.032)。微血管计数与SCCRO或VEGF-A的表达无关,并且不能显着预测存活率。该患者组中的VEGF-A表达是总生存期的预测指标(P <0.032)。结论:在这些原发性人肺鳞癌中VEGF-A表达与SCCRO表达相关,并且是临床行为的预测指标。该数据支持SCRRO和VEGF-A在诱导血管生成中的关联。

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