Immunohistochemical localization of steroid receptor coactivators in chondrosarcoma: An in vivo tissue microarray study

被引:3
作者
Li, Wei [1 ,2 ]
Fu, Jingshu [1 ]
Bian, Chen [3 ]
Zhang, Jiqiang [3 ]
Xie, Zhao [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Orthopaed, Natl & Reg United Engn Lab Tissue Engn, Chongqing 400038, Peoples R China
[2] Bengbu Med Coll, Affiliated Hosp, Dept Orthoped Surg, Bengbu 233030, Anhui, Peoples R China
[3] Third Mil Med Univ, Dept Neurobiol, Chongqing Key Lab Neurobiol, Chongqing 400038, Peoples R China
基金
美国国家科学基金会;
关键词
Chondrosarcoma; SRC-1; SRC-3; Tissue microarray; Immunohistochemistry; BREAST-CANCER METASTASIS; ESTROGEN-RECEPTOR; PROGNOSTIC-SIGNIFICANCE; CELL-MIGRATION; OVARIAN-CANCER; AIB1; EXPRESSION; SRC-1; TUMORS; GENE;
D O I
10.1016/j.prp.2014.04.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Chondrosarcoma is the second most common type of primary bone malignancy following up osteosarcoma, characterized by resistance to conventional chemotherapeutic agents and radiation regimens. The p160 family members steroid receptor coactivator-1 and -3 (SRC-1 and SRC-3) have been implied in the regulation of cancer growth, migration, invasion, metastasis and chemotherapeutic resistance; but we still lack detailed information about the levels of SRCs in chondrosarcoma. In this study, expression of SRC-1 and SRC-3 in chondrosarcoma was examined by immunohistochemistry with tissue microarrays; the four score system (0,1, 2 and 3) was used to evaluate the staining. The results showed that there were no gender-, site-or age-differences regarding the expression of SRC-1 or SRC-3 (p >0.05); organ (bone or cartilage) -differences were only detected for SRC-1 but not SRC-3 (p <0.05). Significant higher levels of SRC-1 and SRC-3 were detected in MDC and PDC when compared to WDC. Our study clearly demonstrated differentiation-dependant expression of SRC-1 and SRC-3 in chondrosarcoma, may be novel targets for the prognosis and/or treatment of chondrosarcoma, would have opened a new avenue and established foundation for studying chondrosarcoma. (C) 2014 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1005 / 1010
页数:6
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