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本文引用的文献

1
Profiles of genomic instability in high-grade serous ovarian cancer predict treatment outcome.高级别浆液性卵巢癌中基因组不稳定性的特征可预测治疗结果。
Clin Cancer Res. 2012 Oct 15;18(20):5806-15. doi: 10.1158/1078-0432.CCR-12-0857. Epub 2012 Aug 21.
2
LRP1B deletion in high-grade serous ovarian cancers is associated with acquired chemotherapy resistance to liposomal doxorubicin.LRP1B 缺失与高级别浆液性卵巢癌对脂质体多柔比星获得性化疗耐药相关。
Cancer Res. 2012 Aug 15;72(16):4060-73. doi: 10.1158/0008-5472.CAN-12-0203.
3
Ovarian cancer risk associated with inherited inflammation-related variants.遗传性炎症相关变异与卵巢癌风险的关联。
Cancer Res. 2012 Mar 1;72(5):1064-9. doi: 10.1158/0008-5472.CAN-11-3512. Epub 2012 Jan 26.
4
Prognostic significance of adhesion molecules (sICAM-1, sVCAM-1) and VEGF in colorectal cancer patients.黏附分子(sICAM-1、sVCAM-1)和 VEGF 在结直肠癌患者中的预后意义。
Thromb Res. 2012 Apr;129(4):e47-50. doi: 10.1016/j.thromres.2011.12.004. Epub 2011 Dec 31.
5
Stem cell pathways contribute to clinical chemoresistance in ovarian cancer.干细胞途径导致卵巢癌临床化疗耐药。
Clin Cancer Res. 2012 Feb 1;18(3):869-81. doi: 10.1158/1078-0432.CCR-11-2188. Epub 2011 Dec 5.
6
VCAM-1 promotes osteolytic expansion of indolent bone micrometastasis of breast cancer by engaging α4β1-positive osteoclast progenitors.VCAM-1 通过与表达α4β1 的破骨细胞祖细胞结合,促进乳腺癌惰性骨微转移的溶骨性扩展。
Cancer Cell. 2011 Dec 13;20(6):701-14. doi: 10.1016/j.ccr.2011.11.002. Epub 2011 Dec 1.
7
Clinical trials and decision-making strategies for optimal treatment of relapsed ovarian cancer.复发性卵巢癌的最佳治疗的临床试验和决策策略。
Eur J Cancer. 2011 Sep;47 Suppl 3:S104-15. doi: 10.1016/S0959-8049(11)70154-X.
8
Rethinking ovarian cancer: recommendations for improving outcomes.重新思考卵巢癌:改善预后的建议。
Nat Rev Cancer. 2011 Sep 23;11(10):719-25. doi: 10.1038/nrc3144.
9
Prognostic value of serum CD44, intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 levels in patients with indolent non-Hodgkin lymphomas.血清 CD44、细胞间黏附分子-1 和血管细胞黏附分子-1 水平对惰性非霍奇金淋巴瘤患者的预后价值。
Leuk Lymphoma. 2012 Jan;53(1):50-6. doi: 10.3109/10428194.2011.616611. Epub 2011 Oct 24.
10
Noninvasive and invasive staging of ovarian cancer: review of the literature.卵巢癌的无创和有创分期:文献复习。
Clin Nucl Med. 2011 Oct;36(10):889-93. doi: 10.1097/RLU.0b013e318219b523.

VCAM1 的表达与高级别浆液性卵巢癌的肿瘤发生和不良预后相关。

VCAM1 expression correlated with tumorigenesis and poor prognosis in high grade serous ovarian cancer.

机构信息

Department of Pathology, The University of Texas MD Anderson Cancer Center Houston, TX, USA ; Department of Pathology, Affiliated Hospital of Nantong University Nantong, Jiangsu, P. R. China.

出版信息

Am J Transl Res. 2013 Apr 19;5(3):336-46. Print 2013.

PMID:23634244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3633976/
Abstract

High expression of vascular cell adhesion molecule 1 (VCAM1) has been shown to be associated with several cancers although its role in ovarian cancer development is largely undefined. The purpose of this study is to investigate its role in ovarian cancer using the epithelial cells and ovarian cancer cell lines and correlate its expression with clinicopathologic parameters in ovarian cancer patients. VCAM1 expression was examined via immunohistochemical staining of 251 high grade serous carcinoma samples using tissue microarray. The expression of VCAM1 was silenced in RAS-transformed ovarian epithelial cell lines and two high grade ovarian cancer cell lines. Cell migration was analyzed in vitro and effect on tumor growth was analyzed in nude mice. High VCAM1 expression was found to be was related with response to surgery and chemotherapy drugs (P = 0.025) and elder age at diagnosis (P = 0.008). Cox regression multivariable analysis showed that VCAM1 expression in tumor cells was an independent prognostic factor. Ovarian cancer cells with VCAM1 overexpression, compared with corresponding control cells, had increased cell migration and enhanced growth of xenograft tumors in mice. Our data provide strong evidence that VCAM1 plays an important role in ovarian tumor growth, and it may be used as a prognostic factor and novel therapeutic target for ovarian cancer.

摘要

血管细胞黏附分子 1(VCAM1)的高表达与多种癌症有关,尽管其在卵巢癌发展中的作用在很大程度上尚未确定。本研究旨在使用上皮细胞和卵巢癌细胞系研究其在卵巢癌中的作用,并将其表达与卵巢癌患者的临床病理参数相关联。使用组织微阵列对 251 例高级别浆液性癌样本进行免疫组织化学染色,检测 VCAM1 的表达。沉默 RAS 转化的卵巢上皮细胞系和两种高级别卵巢癌细胞系中的 VCAM1 表达。在体外分析细胞迁移,并在裸鼠中分析对肿瘤生长的影响。高 VCAM1 表达与手术和化疗药物的反应(P = 0.025)和诊断时的年龄有关(P = 0.008)。Cox 回归多变量分析显示,肿瘤细胞中 VCAM1 的表达是独立的预后因素。与相应的对照细胞相比,过表达 VCAM1 的卵巢癌细胞具有更高的细胞迁移能力,并增强了异种移植肿瘤在小鼠中的生长。我们的数据提供了强有力的证据表明 VCAM1 在卵巢肿瘤生长中起重要作用,它可能被用作卵巢癌的预后因素和新的治疗靶标。