p53 gene mutation in colorectal carcinoma

被引:0
作者
Roa, JC
Roa, I
Melo, A
Araya, JC
Villaseca, MA
Flores, M
Schneider, B
机构
[1] Univ La Frontera, Fac Med, Lab Biol Mol, Temuco, Chile
[2] Univ La Frontera, Unidad Anat Patol, Temuco, Chile
[3] Univ La Frontera, Serv & Dept Cirugia, Temuco, Chile
[4] Univ La Frontera, Hosp Reg Temuco, Temuco, Chile
关键词
carcinoma; colonic neoplasms; p53; gene; mutation; rectal neoplasms;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Genetic events associated to colorectal carcinoma are well characterized, but there is scanty information about this issue in Chilean subjects. Aim: To determine the frequency and distribution of exons 5, 6, 7, 8 and 9 mutations and the immunohistochemical expression of p53 gene in biopsy samples of colorectal carcinoma. Material and methods: p53 gene exons 5, 6, 7, 8 and 9 were directly sequenced in 42 biopsy samples of colorectal carcinoma. Immunohistochemical expression of p53 was determined in 35 samples. Results: Thirty one discrete mutations (12 transitions, 11 transversions and 8 insertions) were observed in 21 samples (60%). Nine samples had mutations in exon 5, twelve samples had mutations in exon 6, seven samples had mutations in exon 7 and three samples had mutations in exons 8 and 9. Immunohistochemical expression of p53 protein was observed in 18 of 35 cases. There was a high correlation between the genetic alteration and immunohistochemistry, when p53 was expressed in more the 20% of cells. The positive and negative predictive values of p53 expression were 87 and 80% respectively. There was a non significant lower mortality among patients with mutations in their biopsies. Conclusions: These results confirm the involvement of p53 gene mutations in colonic carcinogenesis. Immunohistochemical methods for the detection of p53 protein have a high predictive value.
引用
收藏
页码:996 / 1004
页数:9
相关论文
共 40 条
[1]   EVALUATION OF 6 ANTIBODIES FOR IMMUNOHISTOCHEMISTRY OF MUTANT P53 GENE-PRODUCT IN ARCHIVAL COLORECTAL NEOPLASMS [J].
BAAS, IO ;
MULDER, JWR ;
OFFERHAUS, GJA ;
VOGELSTEIN, B ;
HAMILTON, SR .
JOURNAL OF PATHOLOGY, 1994, 172 (01) :5-12
[2]   P53 IMMUNOHISTOCHEMISTRY - A WORD OF CAUTION [J].
BATTIFORA, H .
HUMAN PATHOLOGY, 1994, 25 (05) :435-437
[3]   GENITAL HUMAN PAPILLOMAVIRUS INFECTION IN FEMALE UNIVERSITY-STUDENTS AS DETERMINED BY A PCR-BASED METHOD [J].
BAUER, HM ;
TING, Y ;
GREER, CE ;
CHAMBERS, JC ;
TASHIRO, CJ ;
CHIMERA, J ;
REINGOLD, A ;
MANOS, MM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (04) :472-477
[4]   LOW-FREQUENCY OF P53 MUTATIONS OBSERVED IN A DIVERSE COLLECTION OF PRIMARY HEPATOCELLULAR CARCINOMAS [J].
BUETOW, KH ;
SHEFFIELD, VC ;
ZHU, MH ;
ZHOU, TL ;
SHEN, FM ;
HINO, O ;
SMITH, M ;
MCMAHON, BJ ;
LANIER, AP ;
LONDON, WT ;
REDEKER, AG ;
GOVINDARAJAN, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (20) :9622-9626
[5]  
Burns TF, 1999, J CELL PHYSIOL, V181, P231, DOI 10.1002/(SICI)1097-4652(199911)181:2<231::AID-JCP5>3.0.CO
[6]  
2-L
[7]  
CHO KR, 1992, J CELL BIOCHEM, P137
[8]  
CUNNINGHAM J, 1992, CANCER RES, V52, P1974
[9]   THE CLINICAL RELEVANCE OF THE P53 TUMOR-SUPPRESSOR GENE [J].
DOWELL, SP ;
HALL, PA .
CYTOPATHOLOGY, 1994, 5 (03) :133-145
[10]   The classification of cancer of the rectum [J].
Dukes, CE .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1932, 35 (03) :323-332