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The Expression Profile and Prognostic Significance of Metallothionein Genes in Colorectal Cancer.
Hung, Kuo-Chen; Huang, Tsui-Chin; Cheng, Chia-Hsiung; Cheng, Ya-Wen; Lin, Ding-Yen; Fan, Jhen-Jia; Lee, Kuen-Haur.
Afiliación
  • Hung KC; Division of Gastroenterologic Surgery, Department of Surgery, Yuan's General Hospital, Kaohsiung 80249, Taiwan.
  • Huang TC; Ph.D. Program for Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
  • Cheng CH; Graduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
  • Cheng YW; Department of Biochemistry and Molecular Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
  • Lin DY; Graduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
  • Fan JJ; Cancer Center, Taipei Medical University Hospital, Taipei Medical University, Taipei 11031, Taiwan.
  • Lee KH; Translational Cancer Research Center, Taipei Medical University, Taipei 11031, Taiwan.
Int J Mol Sci ; 20(16)2019 Aug 07.
Article en En | MEDLINE | ID: mdl-31394742
ABSTRACT
Colorectal cancer (CRC) is a heterogeneous disease resulting from the combined influence of many genetic factors. This complexity has caused the molecular characterization of CRC to remain uncharacterized, with a lack of clear gene markers associated with CRC and the prognosis of this disease. Thus, highly sensitive tumor markers for the detection of CRC are the most essential determinants of survival. In this study, we examined the simultaneous downregulation of the mRNA levels of six metallothionein (MT) genes in CRC cell lines and public CRC datasets for the first time. In addition, we detected downregulation of these six MT mRNAs' levels in 30 pairs of tumor (T) and adjacent non-tumor (N) CRC specimens. In order to understand the potential prognostic relevance of these six MT genes and CRC, we presented a four-gene signature to evaluate the prognosis of CRC patients. Further discovery suggested that the four-gene signature (MT1F, MT1G, MT1L, and MT1X) predicted survival better than any combination of two-, three-, four-, five-, or six-gene models. In conclusion, this study is the first to report that simultaneous downregulation of six MT mRNAs' levels in CRC patients, and their aberrant expression together, accurately predicted CRC patients' outcomes.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Perfilación de la Expresión Génica / Transcriptoma / Metalotioneína Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2019 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Perfilación de la Expresión Génica / Transcriptoma / Metalotioneína Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2019 Tipo del documento: Article País de afiliación: Taiwán