Literature DB >> 8872326

Technical approach for the study of the genetic evolution of breast cancer from paraffin-embedded tissue sections.

T Chen1, K Dhingra, A Sahin, N Sneige, G Hortobagyi, C M Aldaz.   

Abstract

We have optimized a technique that allows the study of numerous chromosomal loci (n = 20-50) from single paraffin-embedded tissue sections by microsatellite length polymorphism analysis. DNA samples from normal and breast cancerous tissue can be obtained from the same section by means of microdissection. This technique was further improved by subjecting DNA to several cycles of amplification with a degenerate (universal) primer and then with specific microsatellite primers. This amplified DNA was also used to screen for mutations in the p53 gene by means of PCR-SSCP. In addition adjacent tissue sections were used to assess specific chromosome copy number by interphase cytogenetic analyses (chromosome in situ hybridization) and to analyze expression of specific genes such as p53 and ERBB2. As an example of the use of our approach we performed a detailed chromosome 17 allelotypic analysis in 22 breast tumors (5 ductal carcinomas in situ, 13 invasive ductal carcinomas, and 4 invasive lobular carcinomas). We detected mutations in the p53 gene by PCR-SSCP in 36% of the samples. Samples with significant levels of p53 protein accumulation detected by immunohistochemistry were also positive for mobility shifts in the SSCP analysis. We observed that chromosome 17 allelic losses and imbalance occurred at as early a stage as ductal carcinoma in situ (DCIS). Although in some cases we observed allelic losses or imbalance affecting the 17p13 region, close to the p53 locus, several of the tumors showed dissociation between such loss or imbalance and p53 mutation. Lobular carcinomas were predominantly disomic for chromosome 17 in contrast with ductal tumors, which often showed polysomy for chromosome 17. This comprehensive approach correlating the tumor subtype, its allelotype, with specific chromosome copy number and specific gene mutations and expression in preinvasive or early invasive breast cancer lesions will potentially provide information of relevance for a better understanding of the multistep mechanisms of breast carcinogenesis.

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Year:  1996        PMID: 8872326     DOI: 10.1007/bf01806184

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  22 in total

1.  A second-generation linkage map of the human genome.

Authors:  J Weissenbach; G Gyapay; C Dib; A Vignal; J Morissette; P Millasseau; G Vaysseix; M Lathrop
Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

2.  Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.

Authors:  H Telenius; N P Carter; C E Bebb; M Nordenskjöld; B A Ponder; A Tunnacliffe
Journal:  Genomics       Date:  1992-07       Impact factor: 5.736

3.  Closing in on a breast cancer gene on chromosome 17q.

Authors:  J M Hall; L Friedman; C Guenther; M K Lee; J L Weber; D M Black; M C King
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

4.  Loss of heterozygosity in breast cancer: cause or effect?

Authors:  W L McGuire; S L Naylor
Journal:  J Natl Cancer Inst       Date:  1989-12-06       Impact factor: 13.506

5.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Authors:  M Orita; H Iwahana; H Kanazawa; K Hayashi; T Sekiya
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

Review 6.  Molecular genetic studies of early breast cancer evolution.

Authors:  P O'Connell; V Pekkel; S Fuqua; C K Osborne; D C Allred
Journal:  Breast Cancer Res Treat       Date:  1994       Impact factor: 4.872

7.  Quantitative analysis of chromosome in situ hybridization signal in paraffin-embedded tissue sections.

Authors:  K Dhingra; N Sneige; T K Pandita; D A Johnston; J S Lee; K Emami; G N Hortobagyi; W N Hittelman
Journal:  Cytometry       Date:  1994-06-01

8.  Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms.

Authors:  P A Futreal; P Söderkvist; J R Marks; J D Iglehart; C Cochran; J C Barrett; R W Wiseman
Journal:  Cancer Res       Date:  1992-05-01       Impact factor: 12.701

9.  Clues to the pathogenesis of familial colorectal cancer.

Authors:  L A Aaltonen; P Peltomäki; F S Leach; P Sistonen; L Pylkkänen; J P Mecklin; H Järvinen; S M Powell; J Jen; S R Hamilton
Journal:  Science       Date:  1993-05-07       Impact factor: 47.728

10.  Loss of heterozygosity and p53 gene mutations in breast cancer.

Authors:  G Deng; L C Chen; D R Schott; A Thor; V Bhargava; B M Ljung; K Chew; H S Smith
Journal:  Cancer Res       Date:  1994-01-15       Impact factor: 12.701

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  3 in total

1.  Allelic imbalance at chromosome 17p13.3 (YNZ22) in breast cancer is independent of p53 mutation or p53 overexpression and is associated with poor prognosis at medium-term follow-up.

Authors:  A M Thompson; D N Crichton; R A Elton; M F Clay; U Chetty; C M Steel
Journal:  Br J Cancer       Date:  1998-03       Impact factor: 7.640

Review 2.  Breast cancer and aneusomy 17: implications for carcinogenesis and therapeutic response.

Authors:  Monica M Reinholz; Amy K Bruzek; Daniel W Visscher; Wilma L Lingle; Matthew J Schroeder; Edith A Perez; Robert B Jenkins
Journal:  Lancet Oncol       Date:  2009-03       Impact factor: 41.316

3.  The role of microsatellite instability at chromosome 11p15.5 in the progression of breast ductal carcinoma.

Authors:  Dong-Ja Kim; Ji-Young Park; Myung-Hoon Lee; Yoon-Kyung Sohn
Journal:  J Korean Med Sci       Date:  2004-10       Impact factor: 2.153

  3 in total

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