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SSTR-2、E-cad与不明原因的反复自然流产相关性研究 被引量:3

Correlation between SSTR-2, E-cad and Unexplained Recurrent Spontaneous Abortion
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摘要 目的:研究生长抑素2型受体(SSTR2)、E-钙粘附素(E-cad)与不明原因的反复自然流产相关性。方法:选取2011年1月到2014年12月我院收治的不明原因反复自然流产患者60例(研究组),另选同期早期正常孕妇且准备流产者60例(对照组),应用免疫组化技术检测两组蜕膜组织中的SSTR2和E-cad表达,并进行比较。结果:研究组蜕膜组织中SSTR-2阳性细胞平均光密度显著高于对照组,而E-cad阳性细胞平均光密度显著低于对照组,两组比较差异具有统计学意义(P<0.05);研究组蜕膜组织中SSTR-2与E-cad水平呈负相关关系,对照组蜕膜组织中SSTR-2与E-cad水平呈正相关关系(P<0.05)。结论:蜕膜组织中SSTR-2高表达与E-cad低表达可能与不明原因的反复自然流产有关。 Objective: To study the correlation between somatostatin receptor type 2(SSTR-2), E-cadherin(E-cad) and unexplained recurrent spontaneous abortion. Methods: Selected 60 patients with unexplained recurrent spontaneous abortion from our hospital from January 2011 to December 2014(as study group), and another 60 early normal pregnant who prepared to abort from the same period(as control group), then detected and compared the expression level of SSTR2 and E-cad in deciduas of two groups by immunohistochemistry method. Results: SSTR-2 positive cell mean optical density in study group was significantly higher than control group, but the E-cad positive cell mean optical density was significantly lower than control group, the differences were statistically significant(P〈0.05); Expression level of SSTR-2 was negatively correlated with E-cad in deciduas of study group, while the expression level of SSTR-2 was positively correlated with and E-cad in deciduas of control group(P〈0.05). Conclusion: High expression of SSTR-2and Low expression of E-cad in deciduas may be correlated with unexplained recurrent spontaneous abortion.
出处 《现代生物医学进展》 CAS 2015年第30期5932-5934,共3页 Progress in Modern Biomedicine
基金 河北省计生委科研课题(2011-A21)
关键词 生长抑素2型受体 E-钙粘附素 反复自然流产 SSTR-2 E-cad Recurrent spontaneous abortion
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  • 1Giguere V, Yang N, Segui P, et al. Identification of a new class of steroid hormone receptors. Nature, 1988,331 (6151):91-94.
  • 2Luo I, Sladek R, Carrier I, et al. Reduced fat mass in mice lacking orphan nuclear receptor estrogen-related receptor alpha. Mol Cell BioI, 2003,23(22):7947-7956.
  • 3Shayu D, Rao AI. Expression of functional aromatase in the epididymis: Role of androgens and LH in modulation of expression and activity. Mol Cell Endocrinol, 2006,249(1-2):40-50.
  • 4Vanacker IM, Delmarre C, Guo X, et al. Activation of the osteopontin promoter by the orphan nuclear receptor estrogen receptor related alpha. Cell Growth Differ, 1998,9(12): 1007-1 014.
  • 5Dufour CR, Wilson BJ, Huss JM, et at. Genome-wide orchestration of cardiac functions by the orphan nuclear receptors ERRalpha and gamma. Cell Metab, 2007,5 (5):345-356.
  • 6Stein RA, McDonnell DP. Estrogen-related receptor alpha as a therapeutic target in cancer. Endocr-Relat Cancer, 2006,13:S25-S32.
  • 7Ariazi EA, Kraus RJ, Farrell ML, et al. Estrogen-related receptor alpha 1 transcriptional activities are regulated in part via the ErbB2IHER2 signaling pathway. Mol Cancer Res, 2007,5(1):71-85.
  • 8Boudjadi S, Bematchez G, Beaulieu JF, et al. Control of the human osteopontin promoter by ERRalpha in co1orecta1 cancer. Am J Patho1, 2013,183(1):266-276.
  • 9Lam SS, Mak AS, Yam JW, et at. Targeting estrogen-related receptor alpha inhibits epithelial-tomesenchymal transition and stem cell properties of ovarian cancer cells. Mol Ther, 2014,22(4):743-751.
  • 10Ariazi EA, Clark GM, Mertz JE. Estrogen-related receptor alpha and estrogen-related receptor gamma associate with unfavorable and favorable biomarkers, respectively, in human breast cancer. Cancer Res, 2002,62(22):6510-6518.

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