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let-7i在子宫内膜癌组织中的表达及临床意义 被引量:2

Expression of let-7i in Endometrial Carcinoma and Its Clinical Significance
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摘要 目的:探讨子宫内膜癌组织中let-7i的表达及临床意义。方法:收集2011年4月—2014年12月河北医科大学第一医院40例子宫内膜癌、20例子宫内膜不典型增生及30例正常子宫内膜组织,采用多聚腺苷酸加尾实时荧光定量逆转录聚合酶链反应[poly(A)-RT-q PCR]检测let-7i在不同子宫内膜组织中的表达,并将检测结果和临床及病理资料进行统计学分析。结果:let-7i在子宫内膜癌组织中的表达低于不典型增生和正常子宫内膜组织,3组间差异有统计学意义(P<0.01);不同年龄、病理类型、国际妇产科联盟(FIGO)病理分期、病理分级的子宫内膜癌患者let-7i的表达量差异无统计学意义(P>0.05),在是否合并高血压、糖尿病,是否淋巴结转移及雌激素受体(ER)、孕激素受体(PR)是否阳性的子宫内膜癌患者中let-7i的表达量差异无统计学意义(P>0.05)。结论:let-7i在子宫内膜癌组织中低表达,可能调控了子宫内膜癌的发生。 Objective:To investigate the expression of let-7i in endometrial carcinoma tissues and its clinical significance. Methods: Forty cases of endometrial carcinoma, twenty cases of atypical hyperplasia and thirty cases of normal endometrium tissues were collected from 2011 April to 2014 December at The First Hospital of Hebei Medical University. Poly(A)-RT-q PCR was employed to test the expression of let-7i in different endometrial tissues. The statistical analyses were performed between the expression of let-7i and the clinicopathological characteristics. Results: The expression of let-7i was lower in endometrial carcinoma tissues than that of atypical hyperplasia and normal endometrium tissues, and the difference was statistically significant(P〈0.01). The expression of let-7i in different age, pathological type, FIGO stages, pathological grades of endometrial carcinoma patients had no significant difference(P〉0.05), and its expression in endometrial carcinoma patients whether with hypertension, diabetes, lymph node metastasis and ER-positive, PR-positive had no statistical difference(P〈0.05). Conclusions: The expression of let-7i was down-regulated in endometrial carcinoma tissues, and it may regulate the origination of endometrial carcinoma.
出处 《国际妇产科学杂志》 CAS 2015年第5期588-590,共3页 Journal of International Obstetrics and Gynecology
关键词 子宫内膜肿瘤 微RNAS let-7i 逆转录聚合酶链反应 Endometrial neoplasms Micro RNAs Let-7i Reverse transcriptase polymerase chain reaction
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  • 1Choi HH,Park Y, Choi J,et al. Angiotensin ]1 type I receptor and miR- 155 in endometrial cancers: Synergistic antiproliferative effects of anti-miR-155 and losartan on endometrial cancer cells [J]. Gynecol Oncol, 2012, 126( 1 ): 124-131.
  • 2Yang WH, Lan HY,Tai SK, et al. Repression of bone morphogenetic protein 4 by let-Ti attenuates mesenchymal migration of head and neck cancer'cells[J]. Biochem Biophys Res Commun, 2013,433 ( 1 ) : 24-30.
  • 3Takahashi M, Sung B, Shen Y. Boswellic acid exerts antitumor effects in colorectal cancer cells by modulating expression of the let-7 and miR -200 microRNA family [J]. Carcinogenesis, 2012,133 (12) : 2441-2449.
  • 4Erturk E, Cecener G, Egeli U, et al. Expression status of let-7a and miR-335 among breast tumors in patients with and without germ- line BRCA mutations[J]. Mol Cell Biochem,2014,395(1/2) :77-88.
  • 5饶丽华,黄孝文,许胜.Lin28/Let-7调节环分子机制及相关因子研究进展[J].临床耳鼻咽喉头颈外科杂志,2014,28(9):663-665. 被引量:8
  • 6Xie J,Chen M,Zhou J,et al. MiR-7 inhibits the invasion and metastasis of gastric cancer cells by suppressing epidermal growth factor receptor expression[J]. Oncol Rep,2014,31(4) : 1715-1722.
  • 7Gadducci A,Sergiampietri C,Lanfredini N,et al. Micro-RNAs and ovarian cancer:the state of art and perspectives of clinical research [J]. Gynecol Endocrinol, 2014,30 (4) : 266-271.
  • 8All S,Ahmad A,Ahoukameel A,et al. Increased Ras GTPase activity is regulated by miRNAs that can be attenuated by CDF treatment in pancreatic cancer cells[J]. Cancer Lett, 2012,319 ( 2 ) : 173-181.
  • 9娄雪玲,周梅玲,张占薪,张喜红,姚丽.雌激素受体、孕激素受体、C-erbB-2和Ki-67在子宫内膜癌中的表达及其与临床病理相关性[J].中国实用妇科与产科杂志,2014,30(7):557-560. 被引量:33

二级参考文献29

  • 1谢幸,苟文丽.妇产科学[M].8版.北京:人民卫生出版社,2013:118-119.
  • 2SHAH M S,DAVIDSON L A,CHAPKIN R S.Mechanistic insights into the role of microRNAs in cancer influence of nutrient crosstalk[J].Front Genet,2012,3:305-312.
  • 3REINHART B J,SLACK F J,BASSON M,et al.The 21-nucleotide let-7RNA regulates developmental timing in Caenorhabditis elegans[J].Nature,2000,403:901-906.
  • 4THORNTON J E,GREGORY R I.How does Lin28let-7control development and disease[J]?Trends Cell Biol,2012,22:474-482.
  • 5NAM Y,CHEN C,GREGORY R I,et al.Molecular Basis for interaction of let-7 microRNAs with Lin28[J].Cell,147:1080-1091.
  • 6SAMPSON V B,RONG N H,HAN J,et al.MiRNA let-7adown-regulates MYC and reverts MYC-in-duced growth in Burkitt lymphoma cells[J].Cancer Res,2007,67:9762-9770.
  • 7STITES E C,RAVICHANDRAN K S.A systems perspective of ras signaling in cancer[J].Clin Cancer Res,2009,15:607-611.
  • 8FUSCO A,FEDELE M.Roles of HMGA proteins in cancer[J].Nat Rev Cancer 2007,7:899-910.
  • 9SUMMER H,LI O,BAO Q,et al.HMGA2exhibits dRP/AP site cleavage activity and protects cancer cells from DNA-damage-induced cytotoxicity during chemotherapy[J].Nucleic Acids Res,2009,37:4371-4384.
  • 10NATARAJAN S,HOMBACH-KLONISCH S,DR-GE P,et al.HMGA2inhibits apoptosis through interaction with ATR-CHK1signaling complex in human cancer cells[J].Neoplasia,2013,15:263-280.

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