Literature DB >> 12169679

Multiplex loss of heterozygosity analysis by using single or very few cells.

Xiangfeng Cui1, Helen Feiner, Honghua Li.   

Abstract

Loss of heterozygosity (LOH) is an indication of tumor suppressor gene inactivation. However, loss of heterozygosity analysis has been limited to either a small scale or to very few genetic markers. To significantly increase the scale of study and to include a large number of markers in the analysis, experimental conditions were established for using single cells or single cell equivalent with 10 markers typed simultaneously. Under these conditions, the allele amplification failure rate was 3.7% when single tissue cultured human cells were used. When 30 cells from a 5- micro m paraffin-archived breast tumor tissue section were used, the failure rates were 0% for four of the five heterozygous loci and 10% for the fifth. Small amplification failure rates (6.1% and 6.7% on average) were observed when 5 or 10 cells from paraffin-archived breast tissue were used. These results indicate that with polymerase chain reaction (PCR) primers of high quality, it is possible to obtain reliable results by using single cells from fresh tissue or very few cells from paraffin-archived specimens. The results also show the importance of including replicates, using primers of high quality, and optimizing PCR conditions when a limited amount of material is used for the assay. The feasibility of LOH analysis with very few paraffin-embedded breast cancer tissues was demonstrated.

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Year:  2002        PMID: 12169679      PMCID: PMC1906978          DOI: 10.1016/S1525-1578(10)60699-X

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  23 in total

1.  Whole genome amplification from a single cell: implications for genetic analysis.

Authors:  L Zhang; X Cui; K Schmitt; R Hubert; W Navidi; N Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-01       Impact factor: 11.205

2.  Multiplex genotype determination at a large number of gene loci.

Authors:  Z Lin; X Cui; H Li
Journal:  Proc Natl Acad Sci U S A       Date:  1996-03-19       Impact factor: 11.205

3.  Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA.

Authors:  V G Cheung; S F Nelson
Journal:  Proc Natl Acad Sci U S A       Date:  1996-12-10       Impact factor: 11.205

4.  Multiplex genotype determination at a DNA sequence polymorphism cluster in the human immunoglobulin heavy-chain region.

Authors:  H Li; L Hood
Journal:  Genomics       Date:  1995-03-20       Impact factor: 5.736

5.  Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3.

Authors:  A M Cleton-Jansen; H W Moerland; D F Callen; N A Doggett; P Devilee; C J Cornelisse
Journal:  Cytogenet Cell Genet       Date:  1995

6.  Deletion map of chromosome 16q in ductal carcinoma in situ of the breast: refining a putative tumor suppressor gene region.

Authors:  T Chen; A Sahin; C M Aldaz
Journal:  Cancer Res       Date:  1996-12-15       Impact factor: 12.701

7.  Positional cloning of the Fanconi anaemia group A gene.

Authors: 
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

8.  Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.

Authors:  A Iida; R Isobe; M Yoshimoto; F Kasumi; Y Nakamura; M Emi
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

9.  Allele loss on chromosome 16q24.2-qter occurs frequently in breast cancers irrespectively of differences in phenotype and extent of spread.

Authors:  H Tsuda; D F Callen; T Fukutomi; Y Nakamura; S Hirohashi
Journal:  Cancer Res       Date:  1994-01-15       Impact factor: 12.701

10.  Genetic studies of 457 breast cancers. Clinicopathologic parameters compared with genetic alterations.

Authors:  Y Harada; T Katagiri; I Ito; F Akiyama; G Sakamoto; F Kasumi; Y Nakamura; M Emi
Journal:  Cancer       Date:  1994-10-15       Impact factor: 6.860

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  2 in total

1.  Direct detection of insertion/deletion polymorphisms in an autosomal region by analyzing high-density markers in individual spermatozoa.

Authors:  Sreemanta Pramanik; Honghua Li
Journal:  Am J Hum Genet       Date:  2002-11-19       Impact factor: 11.025

2.  Low copy number DNA template can render polymerase chain reaction error prone in a sequence-dependent manner.

Authors:  Mansour Akbari; Marianne Doré Hansen; Jostein Halgunset; Frank Skorpen; Hans E Krokan
Journal:  J Mol Diagn       Date:  2005-02       Impact factor: 5.568

  2 in total

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