Tumorogenesis and mdm2 protein

被引:0
作者
Flores, C [1 ]
Sobrevia, L [1 ]
机构
[1] Univ Concepcion, Fac Ciencias Biol, Dept Fisiol, CMPL,Lab Fisiol Celular & Mol, Concepcion, Chile
关键词
gene amplification; gene expression regulation; mdm2; oncogenes;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tumorogenesis is associated with several events by which a normal cell transforms itself into a tumour cell with an increased proliferation rate. One of the most important research initiatives in this area is the characterization of the molecular mechanisms involved in tumorogenesis and cancer. Oncogenes and tumour suppressor genes are directly involved in the cell cycle, differentiation, and apoptosis. The cellular oncogene MDM2 seems to be abnormally elevated in several human tumours, specially in sarcomas. The MDM2 gene product, mdm2 protein, pS3 and retinoblastoma (Rb) proteins, play crucial roles in the control of the cell cycle. The molecular interactions between mdm2, pS3 and Rb in cancer, are associated with a loss of control in the G1 phase of the cell cycle leading to uncontrolled cell proliferation. Studies by gene amplification appear to show an incomplete picture of mdm2 protein levels in tumour cells. The simultaneous determination of mdm2 protein and mRNA levels seems to give a more accurate interpretation of the abnormal function of the mdm2 protein. Thus, in addition to gene amplification, different mechanisms by which mdm2 is overexpressed in cancer cells also play an important role in tumorogenesis.
引用
收藏
页码:539 / 546
页数:8
相关论文
共 50 条
[41]   Stress-Induced Isoforms of MDM2 and MDM4 Correlate with High-Grade Disease and an Altered Splicing Network in Pediatric Rhabdomyosarcoma [J].
Jacob, Aishwarya G. ;
O'Brien, Dennis ;
Singh, Ravi K. ;
Comiskey, Daniel F., Jr. ;
Littleton, Robert M. ;
Mohammad, Fuad ;
Gladman, Jordan T. ;
Widmann, Maria C. ;
Jeyaraj, Selvi C. ;
Bolinger, Cheryl ;
Anderson, James R. ;
Barkauskas, Donald A. ;
Boris-Lawrie, Kathleen ;
Chandler, Dawn S. .
NEOPLASIA, 2013, 15 (09) :1049-1063
[42]   Comparison of Chromogenic In Situ Hybridization and Fluorescence In Situ Hybridization for the Evaluation of MDM2 Amplification in Adipocytic Tumors [J].
Mardekian, Stacey K. ;
Solomides, Charalambos C. ;
Gong, Jerald Z. ;
Peiper, Stephen C. ;
Wang, Zi-Xuan ;
Bajaj, Renu .
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2015, 29 (06) :462-468
[43]   MicroRNA-610 is downregulated in glioma cells, and inhibits proliferation and motility by directly targeting MDM2 [J].
Yan, Yu ;
Peng, Yong ;
Ou, Yangzhu ;
Jiang, Yugang .
MOLECULAR MEDICINE REPORTS, 2016, 14 (03) :2657-2664
[44]   Impact of MDM2 polymorphism: increased risk of developing colorectal cancer and a poor prognosis in the Tunisian population [J].
Chaar, Ines ;
Arfaoui, Toumi Amira ;
El Amine, El Hadj Olfa ;
Ben Mahmoud, Lilia ;
Khiari, Mariem ;
Sammoud, Soraya ;
Lounis, Amine ;
Amara, Semeh ;
Gharbi, Lassad ;
Ben Hmida, Abdelmajid ;
Mzabi, Sabeh ;
Bouraoui, Saadia .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2012, 24 (03) :320-327
[45]   Analysis of mdm2 and p53 Gene Alterations in Glioblastomas and its Correlation with Clinical Factors [J].
Martina Schiebe ;
Petra Ohneseit ;
Wolfgang Hoffmann ;
R. Meyermann ;
Hans-Peter Rodemann ;
Michael Bamberg .
Journal of Neuro-Oncology, 2000, 49 :197-203
[46]   Analysis of mdm2 and p53 gene alterations in glioblastomas and its correlation with clinical factors [J].
Schiebe, M ;
Ohneseit, P ;
Hoffmann, W ;
Meyermann, R ;
Rodemann, HP ;
Bamberg, M .
JOURNAL OF NEURO-ONCOLOGY, 2000, 49 (03) :197-203
[47]   MDM2 copy number increase: a poor prognostic, molecular event in esophageal squamous cell carcinoma [J].
Sawada, Ryuichiro ;
Maehara, Ritsuko ;
Oshikiri, Taro ;
Nakamura, Tetsu ;
Itoh, Tomoo ;
Kodama, Yuzo ;
Kakeji, Yoshihiro ;
Zen, Yoh .
HUMAN PATHOLOGY, 2019, 89 :1-9
[48]   CYTOGENETIC EVOLUTION OF MYCN AND MDM2 AMPLIFICATION IN THE NEUROBLASTOMA LS TUMOR AND ITS CELL-LINE [J].
CORVI, R ;
SAVELYEVA, L ;
AMLER, L ;
HANDGRETINGER, R ;
SCHWAB, M .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (04) :520-523
[49]   Immunohistochemical detection of p53 and MDM2 expressions in liposarcoma with World health organization classification [J].
Arici, A. ;
Ozgur, T. ;
Ugras, N. ;
Yalcinkaya, U. .
INDIAN JOURNAL OF CANCER, 2013, 50 (03) :164-169
[50]   MDM2 and CDK4 lmmunohistochemical Coexpression in High-grade Osteosarcoma: Correlation With a Dedifferentiated Subtype [J].
Yoshida, Akihiko ;
Ushiku, Tetsuo ;
Motoi, Toru ;
Beppu, Yasuo ;
Fukayama, Masashi ;
Tsuda, Hitoshi ;
Shibata, Tatsuhiro .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2012, 36 (03) :423-431