HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Expression of the inhibitor of DNA-binding (ID)-1 protein as an angiogenic mediator in tumour advancement of uterine cervical cancers.

Abstract
The ID protein, an inhibitor of basic helix-loop-helix (HLH) transcription factors, has been involved in multiple cellular processes. To investigate the association between tumour advancement and ID expressions of uterine cervical cancers, the levels of ID-1, ID-2 and ID-3 mRNAs were determined by real-time reverse transcription-polymerase chain reaction and the histoscore with the localisation of ID-1 was determined by immunohistochemistry and patient survival in 60 patients. ID-1 histoscores and mRNA levels both significantly (P<0.05) increased in uterine cervical cancers according to clinical stage regardless of histopathological type or lymph node metastasis. Furthermore, the 36-month survival rate of the 30 patients with high ID-1 was poor (60%), whereas that of the other 30 patients with low ID-1 was significantly higher (83%). ID-1 histoscores and mRNA levels significantly (P<0.0001) correlated with microvessel counts in uterine cervical cancers. Tumour cells show mostly diffuse to strong cytoplasmic expression of ID-1 and also very faint expression in endothelial cells. Moreover, ID-1 expression not only correlated with microvessel counts but also correlated significantly with histoscore. Therefore, ID-1 might work on tumour advancement through angiogenic activity and is considered to be a candidate for a prognostic indicator in uterine cervical cancers.
AuthorsM K Maw, J Fujimoto, T Tamaya
JournalBritish journal of cancer (Br J Cancer) Vol. 99 Issue 10 Pg. 1557-63 (Nov 18 2008) ISSN: 1532-1827 [Electronic] England
PMID19002177 (Publication Type: Journal Article)
Chemical References
  • Angiogenesis Modulating Agents
  • Biomarkers, Tumor
  • Inhibitor of Differentiation Protein 1
  • RNA, Messenger
Topics
  • Adenocarcinoma (metabolism)
  • Adult
  • Aged
  • Angiogenesis Modulating Agents (metabolism)
  • Biomarkers, Tumor (metabolism)
  • Carcinoma, Squamous Cell (metabolism)
  • Disease Progression
  • Female
  • Humans
  • Inhibitor of Differentiation Protein 1 (biosynthesis)
  • Middle Aged
  • Neovascularization, Pathologic (metabolism)
  • Prognosis
  • RNA, Messenger
  • Survival Analysis
  • Uterine Cervical Neoplasms (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: