Literature DB >> 9818023

Abnormalities of the FHIT transcripts in osteosarcoma and Ewing sarcoma.

S Hinohara1, N Satake, K Sekine, Y Kaneko.   

Abstract

In a study of FHIT gene abnormalities by reverse transcription-polymerase chain reaction (RT-PCR) and sequence analysis of the PCR products, we found normal and abnormal PCR products in 11 osteosarcomas, one osteosarcoma cell line and 3 Ewing sarcomas, and a normal PCR product only in 5 osteosarcomas and 8 Ewing sarcomas. Sequence analysis of the abnormal PCR products revealed 7 osteosarcomas lacking exons 4 to 6, 7, 8 or 9, two lacking exons 5 to 7 or 10, and two lacking exons 6 to 8 or 10. In the aberrant transcripts of the 11 osteosarcomas, fusion had occurred in the exon/intron junctions in 2 tumors, between a segment within an exon and a complete exon in 3, and between segments within exons in 6. The 3 Ewing sarcomas had lost exon 4 or 5 to exon 6 or 10, and fusion had occurred in the exon/intron junction in one, and between segments within exons in 2. These findings suggest that both abnormal or variant splicing and other mechanisms such as genomic instabilities in the FHIT locus may have resulted in the expression of aberrant transcripts. One osteosarcoma and one cell line established from this osteosarcoma showed different abnormal FHIT transcripts, indicating that the tumor cells with the initial aberrant transcripts may not have had a selective advantage for proliferation. The FHIT abnormalities did not seem to be correlated with lung metastasis or a poor clinical outcome in our patients with osteosarcoma or Ewing sarcoma.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9818023      PMCID: PMC5921954          DOI: 10.1111/j.1349-7006.1998.tb00645.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


  22 in total

1.  Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region.

Authors:  A van den Berg; T G Draaijers; K Kok; T Timmer; A Y Van der Veen; P M Veldhuis; L de Leij; C D Gerhartz; S L Naylor; D I Smith; C H Buys
Journal:  Genes Chromosomes Cancer       Date:  1997-08       Impact factor: 5.006

2.  Variable FHIT transcripts in non-neoplastic tissues.

Authors:  I Panagopoulos; S Thelin; F Mertens; F Mitelman; P Aman
Journal:  Genes Chromosomes Cancer       Date:  1997-08       Impact factor: 5.006

3.  Molecular structure of the human cytoplasmic beta-actin gene: interspecies homology of sequences in the introns.

Authors:  S Nakajima-Iijima; H Hamada; P Reddy; T Kakunaga
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

4.  Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines.

Authors:  S T Ong; K M Fong; S A Bader; J D Minna; M M Le Beau; T W McKeithan; F V Rassool
Journal:  Genes Chromosomes Cancer       Date:  1997-09       Impact factor: 5.006

5.  Molecular cloning of the chromosomal breakpoint of B-cell lymphomas and leukemias with the t(11;14) chromosome translocation.

Authors:  Y Tsujimoto; J Yunis; L Onorato-Showe; J Erikson; P C Nowell; C M Croce
Journal:  Science       Date:  1984-06-29       Impact factor: 47.728

6.  The FHIT gene at 3p14.2 is abnormal in breast carcinomas.

Authors:  M Negrini; C Monaco; I Vorechovsky; M Ohta; T Druck; R Baffa; K Huebner; C M Croce
Journal:  Cancer Res       Date:  1996-07-15       Impact factor: 12.701

7.  Absence of Fhit protein in primary lung tumors and cell lines with FHIT gene abnormalities.

Authors:  G Sozzi; S Tornielli; E Tagliabue; L Sard; F Pezzella; U Pastorino; F Minoletti; S Pilotti; C Ratcliffe; M L Veronese; P Goldstraw; K Huebner; C M Croce; M A Pierotti
Journal:  Cancer Res       Date:  1997-12-01       Impact factor: 12.701

8.  Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines.

Authors:  L Mao; Y H Fan; R Lotan; W K Hong
Journal:  Cancer Res       Date:  1996-11-15       Impact factor: 12.701

9.  Mutation spectrum of the retinoblastoma gene in osteosarcomas.

Authors:  B Wadayama; J Toguchida; T Shimizu; K Ishizaki; M S Sasaki; Y Kotoura; T Yamamuro
Journal:  Cancer Res       Date:  1994-06-01       Impact factor: 12.701

10.  Narrow spectrum of infrequent p53 mutations and absence of MDM2 amplification in Ewing tumours.

Authors:  H Kovar; A Auinger; G Jug; D Aryee; A Zoubek; M Salzer-Kuntschik; H Gadner
Journal:  Oncogene       Date:  1993-10       Impact factor: 9.867

View more
  1 in total

1.  HIF-1α confers aggressive malignant traits on human tumor cells independent of its canonical transcriptional function.

Authors:  Young-Gun Yoo; Jared Christensen; L Eric Huang
Journal:  Cancer Res       Date:  2011-02-08       Impact factor: 12.701

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.