Kirsten Ras* oncogene: Significance of its discovery in human cancer research

被引:54
作者
Tsuchida, Nobuo [1 ]
Murugan, Avaniyapuram Kannan [2 ]
Grieco, Michele [3 ]
机构
[1] Tokyo Med Dent Univ, Grad Sch Med & Dent Sci, Bunkyo Ku, Tokyo, Japan
[2] King Faisal Specialist Hosp & Res Ctr, Dept Mol Oncol, Riyadh, Saudi Arabia
[3] Seconda Univ Napoli, Dipartimento Sci & Tecnol Ambientali Biol & Farma, DiSTABiF, Caserta, Italy
关键词
Kirsten ras; K-ras; KRAS; human cancer; oncogene; EGFR-targeted therapy; MURINE SARCOMA-VIRUS; BLADDER-CARCINOMA ONCOGENE; EGFR-TARGETED THERAPIES; P21 TRANSFORMING PROTEIN; SRC FAMILY KINASES; KRAS CODON 12; COLORECTAL-CANCER; LUNG-CARCINOMA; NUCLEOTIDE-SEQUENCE; ACQUIRED-RESISTANCE;
D O I
10.18632/oncotarget.8773
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The KRAS/K-RAS oncogene is crucially involved in human cancer. The term "oncogene" -i.e., a gene able to transform a normal cell into a tumor cell - was introduced in 1969, but the word was not used in the human carcinogenesis literature until much later. Transforming Kras and Hras oncogenes from the Kirsten and Harvey sarcoma viruses were not identified until the early 1980s due to the complicated structures of the viral genomes. Orthologs of these viral oncogenes were then found in transforming DNA fragments in human cancers in the form of mutated versions of the HRAS and KRAS proto-oncogenes. Thus, RAS genes were the first human oncogenes to be identified. Subsequent studies showed that mutated KRAS acted as an in vivo oncogenic driver, as indicated by studies of anti-EGFR therapy for metastatic colorectal cancers. This review addresses the historical background and experimental studies that led to the discovery of Kirsten Ras as an oncogene, the role of mutated KRAS in human carcinogenesis, and recent therapeutic studies of cancer cells with KRAS mutations.
引用
收藏
页码:46717 / 46733
页数:17
相关论文
共 142 条
[1]   ORIGIN AND BIOLOGICAL PROPERTIES OF A NEW BALB-C MOUSE SARCOMA-VIRUS [J].
AARONSON, SA ;
BARBACID, M .
JOURNAL OF VIROLOGY, 1978, 27 (02) :366-373
[2]   IMPROVED BACTERIAL TEST SYSTEM FOR DETECTION AND CLASSIFICATION OF MUTAGENS AND CARCINOGENS [J].
AMES, BN ;
LEE, FD ;
DURSTON, WE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (03) :782-786
[3]   STRUCTURAL ORGANIZATION AND BIOLOGICAL-ACTIVITY OF MOLECULAR CLONES OF THE INTEGRATED GENOME OF A BALB-C MOUSE SARCOMA-VIRUS [J].
ANDERSEN, PR ;
TRONICK, SR ;
AARONSON, SA .
JOURNAL OF VIROLOGY, 1981, 40 (02) :431-439
[4]   GENERATION OF BALB-MUSV AND HA-MUSV BY TYPE-C VIRUS TRANSDUCTION OF HOMOLOGOUS TRANSFORMING GENES FROM DIFFERENT SPECIES [J].
ANDERSEN, PR ;
DEVARE, SG ;
TRONICK, SR ;
ELLIS, RW ;
AARONSON, SA ;
SCOLNICK, EM .
CELL, 1981, 26 (01) :129-134
[5]   RAT SEQUENCES OF KIRSTEN AND HARVEY MURINE SARCOMA-VIRUS GENOMES - NATURE, ORIGIN, AND EXPRESSION IN RAT TUMOR RNA [J].
ANDERSON, GR ;
ROBBINS, KC .
JOURNAL OF VIROLOGY, 1976, 17 (02) :335-351
[6]   THE AGE DISTRIBUTION OF CANCER AND A MULTI-STAGE THEORY OF CARCINOGENESIS [J].
ARMITAGE, P ;
DOLL, R .
BRITISH JOURNAL OF CANCER, 1954, 8 (01) :1-12
[7]   VIRAL RNA-DEPENDENT DNA POLYMERASE - RNA-DEPENDENT DNA POLYMERASE IN VIRIONS OF RNA TUMOUR VIRUSES [J].
BALTIMORE, D .
NATURE, 1970, 226 (5252) :1209-+
[8]   Amplification of the MET Receptor Drives Resistance to Anti-EGFR Therapies in Colorectal Cancer [J].
Bardelli, Alberto ;
Corso, Simona ;
Bertotti, Andrea ;
Hobor, Sebastijan ;
Valtorta, Emanuele ;
Siravegna, Giulia ;
Sartore-Bianchi, Andrea ;
Scala, Elisa ;
Cassingena, Andrea ;
Zecchin, Davide ;
Apicella, Maria ;
Migliardi, Giorgia ;
Galimi, Francesco ;
Lauricella, Calogero ;
Zanon, Carlo ;
Perera, Timothy ;
Veronese, Silvio ;
Corti, Giorgio ;
Amatu, Alessio ;
Gambacorta, Marcello ;
Diaz, Luis A., Jr. ;
Sausen, Mark ;
Velculescu, Victor E. ;
Comoglio, Paolo ;
Trusolino, Livio ;
Di Nicolantonio, Federica ;
Giordano, Silvia ;
Siena, Salvatore .
CANCER DISCOVERY, 2013, 3 (06) :658-673
[9]   GENETIC MECHANISMS IN TUMOR INITIATION AND PROGRESSION .10. THE RAS GENE FAMILY AND HUMAN CARCINOGENESIS [J].
BOS, JL .
MUTATION RESEARCH, 1988, 195 (03) :255-271
[10]  
BOS JL, 1989, CANCER RES, V49, P4682