Increased muscle ubiquitin mRNA levels in gastric cancer patients

被引:114
作者
Bossola, M
Muscaritoli, M
Costelli, P
Bellantone, R
Pacelli, F
Busquets, S
Argilès, J
Lopez-Soriano, FJ
Civello, IM
Baccino, FM
Fanelli, FR
Doglietto, GB
机构
[1] Univ Cattolica Sacro Cuore, Ist Clin Chirurg, I-00168 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Med Clin, Rome, Italy
[3] Univ Turin, Dipartimento Med & Oncol Sperimentale, Turin, Italy
[4] Ctr Consiglio Nazl Ric Immunogenet & Oncol Sperim, Turin, Italy
[5] Univ Barcelona, Dept Bioquim & Biol, Barcelona, Spain
关键词
cachexia; protein breakdown; proteolytic pathways;
D O I
10.1152/ajpregu.2001.280.5.R1518
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The intramuscular ATP-dependent ubiquitin (Ub)-proteasome proteolytic system is hyperactivated in experimental cancer cachexia. The present study aimed at verifying whether the expression of the muscle Ub mRNA is altered in patients with cancer. Total muscle RNA was extracted using the guanidinium isothiocyanate/phenol/chloroform method from rectus abdominis biopsies obtained intraoperatively from 20 gastric cancer (GC) patients and 10 subjects with benign abdominal diseases (CON) undergoing surgery. Ub mRNA levels were measured by northern blot analysis. Serum soluble tumor necrosis factor receptor (sTNFR) was measured by ELISA. Ub mRNA levels (arbitrary units, means +/- SD) were 2,345 +/- 195 in GC and 1,162 +/- 132 in CON (P = 0.0005). Ub mRNA levels directly correlated with disease stage (r = 0.608, P = 0.005), being 1,945 +/- 786 in stages I and II, 2,480 +/- 650 in stage III, and 3,799 +/- 66 in stage IV. Ub mRNA and sTNFR did not correlate with age and nutritional parameters. This study confirms experimental data indicating an overexpression of muscle Ub mRNA in cancer cachexia. Lack of correlation with nutritional status suggests that Ub activation in human cancer is an early feature that precedes any clinical sign of cachexia.
引用
收藏
页码:R1518 / R1523
页数:6
相关论文
共 42 条
  • [1] ADERKA D, 1985, LANCET, V2, P1190
  • [2] Argilés JM, 1999, INT J ONCOL, V14, P479
  • [3] BALKWILL F, 1987, LANCET, V2, P1229
  • [4] ACTIVATION OF THE ATP-UBIQUITIN-PROTEASOME PATHWAY IN SKELETAL-MUSCLE OF CACHECTIC RATS BEARING A HEPATOMA
    BARACOS, VE
    DEVIVO, C
    HOYLE, DHR
    GOLDBERG, AL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 268 (05): : E996 - E1006
  • [5] Contribution of the ubiquitin-proteasome pathway to overall muscle proteolysis in hypercatabolic patients
    Biolo, G
    Bosutti, A
    Iscra, F
    Toigo, G
    Gullo, A
    Guarnieri, G
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (06): : 689 - 691
  • [6] UBIQUITIN IS A HEAT-SHOCK PROTEIN IN CHICKEN-EMBRYO FIBROBLASTS
    BOND, U
    SCHLESINGER, MJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (05) : 949 - 956
  • [7] Calpain: A protease in search of a function?
    Carafoli, E
    Molinari, M
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 247 (02) : 193 - 203
  • [8] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [9] THE UBIQUITIN-PROTEASOME PROTEOLYTIC PATHWAY
    CIECHANOVER, A
    [J]. CELL, 1994, 79 (01) : 13 - 21
  • [10] TUMOR-NECROSIS-FACTOR-ALPHA MEDIATES CHANGES IN TISSUE PROTEIN-TURNOVER IN A RAT CANCER CACHEXIA MODEL
    COSTELLI, P
    CARBO, N
    TESSITORE, L
    BAGBY, GJ
    LOPEZSORIANO, FJ
    ARGILES, JM
    BACCINO, FM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) : 2783 - 2789