Cyclic guanosine monophosphate phosphodiesterase activity in human gingival carcinoma

被引:10
作者
Spoto, G
Fioroni, M
Rubini, C
Contento, A
Di Nicola, M
Forcella, S
Piattelli, A
机构
[1] Univ G DAnnunzio, Dept Appl Sci Oral & Dent Dis, Sch Med, I-66013 Chieti, Italy
[2] Univ Ancona, Inst Pathol Anat & Histopathol, Ancona, Italy
关键词
cGMP; oral squamous cell carcinomas; phosphodiesterase;
D O I
10.1034/j.1600-0714.2003.00083.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: Cyclic guanosine monophosphate (cGMP) is an essential second messenger metabolized by phosphodiesterases (PDEs). Objectives: We looked for a possible correlation of PDE activities in human oral squamous cell carcinoma (OSCC) with and without lymph node metastases. Materials and methods: The analysis of phosphodiesterase activity and the cGMP assay were done by reverse-phase HPLC on samples of fresh or frozen gingival tissues. Analysis of cGMP was confirmed with the enzyme-linked immunoabsorption assay. Results and conclusions: cGMP PDE activity was 34.92+/-7.17 SD, 12.89+/-4.43 SD, and 35.88+/-8.76 SD (nmols/mg of protein), respectively, in controls, samples without lymph node involvement (N-), and specimens with lymph node metastases (N+). cGMP values were 1.97+/-0.63 SD, 3.30+/-1.47 SD, and 3.49+/-1.47 SD (nmols/mg of protein). Our data support the hypothesis of a role for cGMP and PDE in the progression of OSCC.
引用
收藏
页码:189 / 194
页数:6
相关论文
共 34 条
[1]  
BEAVO JA, 1988, ADV SEC MESS PHOSPH, V22, P1
[2]   METABOLISM OF GUANINE AND GUANINE-NUCLEOTIDES IN PRIMARY RAT NEURONAL CULTURES [J].
BROSH, S ;
SPERLING, O ;
DANTZIGER, E ;
SIDI, Y .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (04) :1485-1490
[3]   CYCLIC NUCLEOTIDE PHOSPHODIESTERASE ACTIVITY IN MUSCLE OF PATIENTS WITH CARCINOMA [J].
CANAL, N ;
CERRI, C ;
FRATTOLA, L ;
TRABUCCHI, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1979, 43 (03) :421-427
[4]   APOPTOSIS AND DISEASE [J].
CARSON, DA ;
RIBEIRO, JM .
LANCET, 1993, 341 (8855) :1251-1254
[5]   ACTIVATION OF INTESTINAL CFTR CL- CHANNEL BY HEAT-STABLE ENTEROTOXIN AND GUANYLIN VIA CAMP-DEPENDENT PROTEIN-KINASE [J].
CHAO, AC ;
DESAUVAGE, FJ ;
DONG, YJ ;
WAGNER, JA ;
GOEDDEL, DV ;
GARDNER, P .
EMBO JOURNAL, 1994, 13 (05) :1065-1072
[6]  
CURTISPRIOR PB, 1976, LANCET, V2, P1224
[7]   Cyclic-3′,5′-nucleotide phosphodiesterase isozymes in cell biology and pathophysiology of the kidney [J].
Dousa, TP .
KIDNEY INTERNATIONAL, 1999, 55 (01) :29-62
[8]  
DREES M, 1993, CANCER RES, V53, P3058
[9]   Molecular cloning and characterization of a distinct human phosphodiesterase gene family: PDE11A [J].
Fawcett, L ;
Baxendale, R ;
Stacey, P ;
McGrouther, C ;
Harrow, I ;
Soderling, S ;
Hetman, J ;
Beavo, JA ;
Phillips, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3702-3707
[10]   Isolation and characterization of PDE9A, a novel human cGMP-specific phosphodiesterase [J].
Fisher, DA ;
Smith, JF ;
Pillar, JS ;
St Denis, SH ;
Cheng, JB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15559-15564