期刊文献+

HPIP蛋白与恶性肿瘤关系的研究进展

Progress of the relationship between HPIP and cancer
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摘要 随着肿瘤分子生物学的飞速发展,分子靶向治疗已成为肿瘤治疗方法中最具前景的研究领域,分子靶点的研究也早已成为医学界关注的热点。人造血相关的PBX相互作用蛋白质(HPIP)是一种新型的支架蛋白。近年来根据相关文献报道,HPIP与肿瘤生的长、增殖和转移密切相关,有可能成为肿瘤治疗的新靶点。本文总结了HPIP在恶性肿瘤发展中的作用及其相关机制的研究进展。 With the rapid development of tumor molecular biology,molecular targeted therapy has become the most promising treatment of cancer and the study of molecular targets has been to be a hot topic for a long time. Remarkably,hematopoietic Pbx-interaction protein( HPIP),a microtubule-binding protein,is a novel scaffolding protein. To date,according to the relevant literature,HPIP is closely associated with tumor growth,proliferation and metastasis. HPIP may be a new target for cancer therapy in the future.We review a representative set of resent studies and summarizes the progress of mechanisms and significance of HPIP in the development of malignant tumors.
出处 《临床肿瘤学杂志》 CAS 2015年第1期83-86,共4页 Chinese Clinical Oncology
基金 国家自然科学基金青年基金资助项目(81302067)
关键词 造血相关的PBX相互作用蛋白质基因(HPIP) 分子靶向治疗 进展 Hematopoietic PBX-interacting protein Molecular targeted therapy Progress
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参考文献20

  • 1Siegel R, Ma J, Zou Z, et al. Cancer statistics, 20,14 [ J ]. CA Cancer J Clin, 2014, 64(1): 9-29.
  • 2Okada S, Irie T, Tanaka J, et al. Potential role of hematopoietic pre-B-cell leukemia transcription factor-interacting protein in oral carcinogenesis [ J ]. J Oral Pathol Med, 2014,23 (6) : 17-25.
  • 3Karamese M, Aksak S, Gundogdu OB, et al. A new hypothesis a- bout hematopoietic Pbx-interaction protein ( HPIP ) : can it be a key factor in neurodegeneration in the post-menopausal period.'? [J]. Med Hypotheses, 2013, 81(3): 470-476.
  • 4Abramo,Jich C, Chavez EA, Lansdorp PM, et at. Functional characterization of multiple domains involved in the subcellular lo- calization of the hematopoietic Pbx interacting protein ( HPIP ) [J]. Oneogene, 2002, 21(44): 6766-6771.
  • 5Manavathi B, Lo D, Bugide S, et al. Functional regulation of pre- B-cell leukemia homeobox interacting protein 1 (PBXIP1/HPIP) in erythroid differentiation [ J ]. J Biol Chem, 2012, 287 ( 8 ) : 5600-5614.
  • 6Boonyaratanakornkit V. Scaffolding proteins mediating membrane- initiated extra-nuclear actions of estrogen receptor [ J ]. Steroids, 2011, 76(9): 877-884.
  • 7Abramovich C, Shen WF, Pineault N, et al. Functional cloning and characterization of a novel nonhomeodomain protein that in- hibits the binding of PBX1-HOX complexes to DNA [ J]. J Biol Chem, 2000, 275(34): 26172-26177.
  • 8Xu X, Fan Z, Kang L, et al. Hepatitis B virus X protein represses miRNA-148a to enhance tumorigenesis [ J ]. J Clin Invest, 2013, 123(2): 630-645.
  • 9Manavathi B, Acconcia F, Rayala SK, et al. An inherent role of microtubule network in the action of nuclear receptor [ J ]. Proc Natl Aead Sci U S A, 2006, 103(43) : 15981-15986.
  • 10徐小洁,王凌雪,范忠义,丁丽华,张浩,杨智洪,李杰之,叶棋浓.敲减人HPIP基因表达抑制细胞生长增殖[J].中国生物化学与分子生物学报,2011,27(2):190-196. 被引量:3

二级参考文献104

  • 1Abramovich C, Shen W F, Pineault N, et al. Functional cloning and characterization of a novel nonhomeodomain protein that inhibits the binding of PBX1-HOX complexes to DNA[ J]. J Biol Chem ,2000,275 ( 34 ) :26172-26177.
  • 2Abramovich C, Chavez E A, Lansdorp P M, et al. Functional characterization of multiple domains involved in the subcellular localization of the hematopoietic Pbx interacting protein (HPIP) [ J]. Oncogene ,2002,21 (44) :6766-6771.
  • 3Lu Q, Kamps M P. Heterodimerization of Hox prateins with Pbx1 and oncoprotein E2a-Pbx1 generates unique DNA-binding specifities at nucleotides predicted to contact the N-terminal arm of the Hox homeodomain--demonstration of Hox-dependent largeting of E2a-pbxl in vivo [ J ]. Oncogene, 1997, 14 ( 1 ) :75- 83.
  • 4Manavathi B,Acconcia F, Rayala S K,et al.. An inherent role of microtubule network in the action of nuclear receptor [J]. Proc Natl Acad Sci U S A,2006,103(43) :15981-15986.
  • 5Banan M ,Puri N. The ins and outs of RNAi in mammalian ceils [ J ]. C urr Pharm Biotechnol,2004,5 ( 5 ) :441 -450.
  • 6Yu J Y, DeRuiter S L, Turner D L. RNA interference by expression of short-interfering RNAs and hairpin RNAs in mammalian cells[ J]. Proc Natl Acad Sci U S A, 2002,99 ( 9 ) : 6047-6052.
  • 7Lee N S, Dohjima T, Bauer G, et al. Expression of small interfering RNAs targeted against HIV-1 rev transcripts in human cells [ J ]. Nat Bioteehnol, 2002,20 ( 5 ) : 500-505.
  • 8Miyagishi M, Taira K. U6 promoter-driven siRNAs with four uridine 3'overhangs efficiently suppress targeted gene expression in mammalian cells[J]. Nat Biotechnol,2002,20(5) :497-500.
  • 9Brummelkamp T R, Bernards R, Agami R. A system for stable expression of short interfering RNAs in mammalian cells [ J ]. Science,2002,296(5567) :550-553.
  • 10Ortiz-Quintero B. RNA interference: from origins to a novel tool for gene silencing [J]. Rev Invest Clin,2009,61(5) :412-427.

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