Nucleostemin mRNA is expressed in both normal and malignant renal tissues

被引:35
作者
Fan, Y.
Liu, Z.
Zhao, S.
Lou, F.
Nilsson, S.
Ekman, P.
Xu, D.
Fang, X.
机构
[1] Karolinska Univ Hosp, Div Hematol, Dept Surg, Div Urol, SE-17176 Stockholm, Sweden
[2] Karolinska Univ Hosp, Div Hematol, Dept Oncol Pathol, SE-17176 Stockholm, Sweden
[3] Karolinska Univ Hosp, Div Hematol, Dept Med, SE-17176 Stockholm, Sweden
[4] Shandong Univ, Dept Urol, Qilu Hosp, Jinan 250012, Peoples R China
[5] Shandong Univ, Sch Nursing, Aging & Hlth Ctr, Jinan 250012, Peoples R China
[6] Shandong Univ, Inst Urol, Jinan 250012, Peoples R China
关键词
nucleostemin; RCC; renal tissues; c-MYC;
D O I
10.1038/sj.bjc.6603145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nucleostemin (NS), a p53-binding protein, has been shown essential for stem and cancer cell proliferation and implicated in oncogenesis. To explore potential contributions of NS to the development of clear cell renal cell carcinomas (ccRCCs), we determined NS expression in ccRCC cell lines, and in paired normal and malignant renal tissues from 31 patients with ccRCC. Nucleostemin mRNA and/or protein expression was observed in all four cell lines and 27 of 31 (87%) tumour specimens. Surprisingly, 16 of 31 (52%) adjacent normal renal samples also expressed NS mRNA and its levels in four of them were comparable with those in paired tumour tissues. Three of the patients had detectable NS mRNA in their normal renal tissues whereas lacked its expression in the matched tumours. Compared to the oncogene c-MYC expression in these same samples, NS expression showed a much less specificity for ccRCC. We further demonstrated that NS mRNA expression was closely associated with cellular proliferation in normal fibroblasts or T lymphocytes and renal cell carcinoma cell lines. Collectively, NS expression widely occurs in normal and malignant renal tissues, and is likely a proliferation marker rather than a unique regulator of cell proliferation and survival in stem and cancer cells.
引用
收藏
页码:1658 / 1662
页数:5
相关论文
共 27 条
[1]  
Brauch H, 2000, CANCER RES, V60, P1942
[2]   Caveolin-1 overexpression predicts poor disease-free survival of patients with clinically confined renal cell carcinoma [J].
Campbell, L ;
Gumbleton, M ;
Griffiths, DFR .
BRITISH JOURNAL OF CANCER, 2003, 89 (10) :1909-1913
[3]  
DONKSOV F, 2006, BRIT J CANCER, V94, P218
[4]   Mcm2, Geminin, and Ki67 define proliferative state and are prognostic markers in renal cell carcinoma [J].
Dudderidge, TJ ;
Stoeber, K ;
Loddo, M ;
Atkinson, G ;
Fanshawe, T ;
Griffiths, DF ;
Williams, GH .
CLINICAL CANCER RESEARCH, 2005, 11 (07) :2510-2517
[5]   Reassessment of the 1997 TNM classification system for renal cell carcinoma - A 5-cm T1/T2 cutoff is a better predictor of clinical outcome [J].
Elmore, JM ;
Kadesky, KT ;
Koeneman, KS ;
Sagalowsky, AI .
CANCER, 2003, 98 (11) :2329-2334
[6]   Differential expression of full-length telomerase reverse transcriptase mRNA and telomerase activity between normal and malignant renal tissues [J].
Fan, YD ;
Liu, ZX ;
Fang, XL ;
Ge, Z ;
Ge, N ;
Jia, Y ;
Sun, P ;
Lou, FL ;
Björkholm, M ;
Gruber, A ;
Ekman, P ;
Xu, DW .
CLINICAL CANCER RESEARCH, 2005, 11 (12) :4331-4337
[7]   SOMATIC MUTATIONS OF THE VON HIPPEL-LINDAU DISEASE TUMOR-SUPPRESSOR GENE IN NONFAMILIAL CLEAR-CELL RENAL-CARCINOMA [J].
FOSTER, K ;
PROWSE, A ;
VANDENBERG, A ;
FLEMING, S ;
HULSBEEK, MMF ;
CROSSEY, PA ;
RICHARDS, FM ;
CAIRNS, P ;
AFFARA, NA ;
FERGUSONSMITH, MA ;
BUYS, CHCM ;
MAHER, ER .
HUMAN MOLECULAR GENETICS, 1994, 3 (12) :2169-2173
[8]   Transient induction of metallothionein isoform 3 (MT-3), c-fos, c-jun and c-myc in human proximal tubule cells exposed to cadmium [J].
Garrett, SH ;
Phillips, V ;
Somji, S ;
Sens, MA ;
Dutta, R ;
Park, S ;
Kim, D ;
Sens, DA .
TOXICOLOGY LETTERS, 2002, 126 (01) :69-80
[9]   Therapeutic options in the management of renal cell carcinoma [J].
Glaspy, JA .
SEMINARS IN ONCOLOGY, 2002, 29 (03) :41-46
[10]   MUTATIONS OF THE VHL TUMOR-SUPPRESSOR GENE IN RENAL-CARCINOMA [J].
GNARRA, JR ;
TORY, K ;
WENG, Y ;
SCHMIDT, L ;
WEI, MH ;
LI, H ;
LATIF, F ;
LIU, S ;
CHEN, F ;
DUH, FM ;
LUBENSKY, I ;
DUAN, DR ;
FLORENCE, C ;
POZZATTI, R ;
WALTHER, MM ;
BANDER, NH ;
GROSSMAN, HB ;
BRAUCH, H ;
POMER, S ;
BROOKS, JD ;
ISAACS, WB ;
LERMAN, MI ;
ZBAR, B ;
LINEHAN, WM .
NATURE GENETICS, 1994, 7 (01) :85-90