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[The expression and clinical implication of inducible nitric oxide synthase mRNA in laryngeal carcinoma and hypopharyngeal carcinoma].

AbstractOBJECTIVE:
To study the expression of inducible nitric oxide synthase(iNOS) mRNA in laryngeal carcinoma and hypopharyngeal carcinoma and its clinical significance.
METHOD:
The tissue samples (laryngeal carcinoma, 40; hypopharyngeal carcinoma, 12; adjacent tissue, 50; laryngeal papilloma, 10; amyloidosis of larynx, 2; and normal laryngeal mucosa, 7) were examined by reverse transcription-polymerase chain reaction(RT-PCR).
RESULT:
1. The target gene of iNOS were detected in 41 of 52 tumor tissues, 10 of 50 adjacent tissues, 5 of 12 benign tumor tissues and 0 of 7 normal tissues. The difference was significant (P < 0.0001, P < 0.005, P < 0.0001); 2. No significant difference was found among the expression of iNOSmRNA in different primary locations, there was significant statistical difference between the early clinical stages (T1-T2) and the advanced stages (T3-T4); 3. The poorly differentiated tumor cell showed a higher iNOSmRNA expression than that in moderate differentiated tumor cell (P < 0.05) and the iNOSmRNA expression in the lymph node metastasis group was higher than the non-metastasis group (P < 0.05).
CONCLUSION:
It suggests that iNOS gene expression occurs in human laryngeal carcinoma and hypopharyngeal carcinoma, it might involve in the development of head and neck neoplasms in gene level by generating NO.
AuthorsXiaodong Du, Xinyong Luan, Xinliang Pang, Chang Shu, Feng Wang, Jindong Ren, Chaohui Huang
JournalLin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology (Lin Chuang Er Bi Yan Hou Ke Za Zhi) Vol. 17 Issue 10 Pg. 612-4 (Oct 2003) China
PMID14727435 (Publication Type: English Abstract, Journal Article)
Chemical References
  • RNA, Messenger
  • NOS2 protein, human
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
Topics
  • Aged
  • Female
  • Humans
  • Hypopharyngeal Neoplasms (genetics, metabolism)
  • Laryngeal Neoplasms (genetics, metabolism)
  • Male
  • Middle Aged
  • Nitric Oxide Synthase (biosynthesis, genetics)
  • Nitric Oxide Synthase Type II
  • Papilloma (genetics, metabolism)
  • RNA, Messenger (biosynthesis, genetics)
  • Reverse Transcriptase Polymerase Chain Reaction

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