期刊文献+

microRNA-32在多发性骨髓瘤中的表达及临床意义(英文)

Expression and significance of microRNA-32 in multiple myeloma
下载PDF
导出
摘要 Objective: This study was aimed to explore the expression of microRNA-32(miR-32) in multiple myeloma(MM), and study its association with β2-microglobulin and staging of MM by Durie-Salmon classification. Methods: The expression level of miR-32 in bone marrow mono-nuclear cells of MM were examined by real-time polymerase chain reaction(real-time PCR), and the correlations between the expression level of miR-32 and related clinic pathologic features β2-microglobulin, staging of MM by Durie-Salmon classification were further analyzed. Results: The expression of miR-32 in MM patients was obviously higher than that in normal control(P < 0.05). The expression of miR-32 in relapsed/ refractory MM patients was obviously higher than that in newly diagnosed MM patients. The expression of miR-32 in MM patients decreased after chemical therapy than that before treatment, especially in effective group(P < 0.05). There was no statistically significant change in ineffective/progress group after chemical therapy(P > 0.05).The expression of miR-32 was associated to staging of MM and β2-microglobulin level. Conclusion: Expression level of miR-32 in MM patients is significantly higher than that in normal bone marrow, these data indicated that miR-32 may play an important role in the development of MM. High-regulated expression of miR-32 was associated with β2-microglobulin and staging of MM by Durie-Salmon classification. Objective: This study was aimed to explore the expression of microRNA-32(miR-32) in multiple myeloma(MM), and study its association with β2-microglobulin and staging of MM by Durie-Salmon classification. Methods: The expression level of miR-32 in bone marrow mono-nuclear cells of MM were examined by real-time polymerase chain reaction(real-time PCR), and the correlations between the expression level of miR-32 and related clinic pathologic features β2-microglobulin, staging of MM by Durie-Salmon classification were further analyzed. Results: The expression of miR-32 in MM patients was obviously higher than that in normal control(P 0.05). The expression of miR-32 in relapsed/ refractory MM patients was obviously higher than that in newly diagnosed MM patients. The expression of miR-32 in MM patients decreased after chemical therapy than that before treatment, especially in effective group(P 0.05). There was no statistically significant change in ineffective/progress group after chemical therapy(P 0.05).The expression of miR-32 was associated to staging of MM and β2-microglobulin level. Conclusion: Expression level of miR-32 in MM patients is significantly higher than that in normal bone marrow, these data indicated that miR-32 may play an important role in the development of MM. High-regulated expression of miR-32 was associated with β2-microglobulin and staging of MM by Durie-Salmon classification.
出处 《The Chinese-German Journal of Clinical Oncology》 CAS 2014年第10期472-475,共4页 中德临床肿瘤学杂志(英文版)
基金 Supported by grants from the Qingdao Public Sphere Support Program of Qingdao Municipal Science and Technology Commission(No.2010KZJ-9) Qingdao Public Health Bureau(No.2012-WSZD042)
关键词 多发性骨髓瘤 实时PCR 聚合酶链反应 化学治疗 球蛋白 单核细胞 病理特征 化学疗法 microRNA-32(miR-32) multiple myeloma(MM) real-time polymerase chain reaction(real-time PCR)
  • 相关文献

参考文献1

二级参考文献10

  • 1Rebecca Siegel,Deepa Naishadham,Ahmedin Jemal.Cancer statistics, 2013[J]. CA: A Cancer Journal for Clinicians . 2013 (1)
  • 2Shin Hamada,Kennichi Satoh,Shin Miura,Morihisa Hirota,Atsushi Kanno,Atsushi Masamune,Kazuhiro Kikuta,Kiyoshi Kume,Jun Unno,Shinichi Egawa,Fuyuhiko Motoi,Michiaki Unno,Tooru Shimosegawa.miR‐197 induces epithelial–mesenchymal transition in pancreatic cancer cells by targeting p120 catenin[J]. J. Cell. Physiol. . 2013 (6)
  • 3Amy L. Collins,Sylwia Wojcik,James Liu,Wendy L. Frankel,Hansjuerg Alder,Lianbo Yu,Thomas D. Schmittgen,Carlo M. Croce,Mark Bloomston.A Differential MicroRNA Profile Distinguishes Cholangiocarcinoma from Pancreatic Adenocarcinoma[J].Annals of Surgical Oncology.2014(1)
  • 4Christian Marin-Muller,Dali Li,Uddalak Bharadwaj,Min Li,Changyi Chen,Sally E. Hodges,William E. Fisher,Qianxing Mo,Mien-Chie Hung,Qizhi Yao.A Tumorigenic Factor Interactome Connected through Tumor Suppressor MicroRNA-198 in Human Pancreatic Cancer[J].Clinical Cancer Research.2013(21)
  • 5Marine Humeau,Jér?me Torrisani,Pierre Cordelier.miRNA in clinical practice: Pancreatic cancer[J].Clinical Biochemistry (-).2013(10-11)
  • 6Gang Zhao,Bo Wang,Yang Liu,Jun-gang Zhang,Shi-chang Deng,Qi Qin,Kui Tian,Xiang Li,Shuai Zhu,Yi Niu,Qiong Gong,Chun-you Wang.miRNA-141, Downregulated in Pancreatic Cancer, Inhibits Cell Proliferation and Invasion by Directly Targeting MAP4K4[J].Molecular Cancer Therapeutics.2013(11)
  • 7Tiffany N. MacKenzie,Nameeta Mujumdar,Sulagna Banerjee,Veena Sangwan,Aaron Sarver,Selwyn Vickers,Subbaya Subramanian,Ashok K. Saluja.Triptolide Induces the Expression of miR-142-3p: A Negative Regulator of Heat Shock Protein 70 and Pancreatic Cancer Cell Proliferation[J].Molecular Cancer Therapeutics.2013(7)
  • 8Saurabh Singh,Deepak Chitkara,Virender Kumar,Stephen W. Behrman,Ram I. Mahato.miRNA profiling in pancreatic cancer and restoration of chemosensitivity[J].Cancer Letters.2013(2)
  • 9Hiroaki Nagano,Yoshito Tomimaru,Hidetoshi Eguchi,Naoki Hama,Hiroshi Wada,Koichi Kawamoto,Shogo Kobayashi,Masaki Mori,Yuichiro Doki.MicroRNA-29a induces resistance to gemcitabine through the Wnt/β-cateninsignaling pathway in pancreatic cancer cells[J].International Journal of Oncology.2013(4)
  • 10Gianpiero Di Leva,Carlo M Croce.miRNA profiling of cancer[J].Current Opinion in Genetics & Development.2013(1)

共引文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部