Literature DB >> 30390187

Evaluation genotypes of cancer cell lines HCC1954 and SiHa by short tandem repeat (STR) analysis and DNA sequencing.

Jiewen Fu1,2, Jingliang Cheng1,2, Xiaoyan Liu1, Jun Li1, Chunli Wei1, Xiaoli Zheng2, Tao He3,4, Junjiang Fu5,6.   

Abstract

Cancer cell lines are used worldwide in biomedical researches, and data interpretation solely depends on unambiguous attribution of those respective cell lines to its original sources. Approximately one-third of all cell lines have an origin other than that assumed, leading to invalid results. It is necessary to characterize the origin of cell lines. Short-tandem-repeat (STR) fingerprinting (DNA fingerprinting) is the method for characterization of genetic identity in cultured cell lines under certain experimental conditions. We showed the fingerprinting profiles in a summed and unidentified human cancer cell line comparison to HCC1954 cell line, revealing marked alterations in DNA fingerprinting profiles up to fourteen STR loci from 16 loci. Furthermore, Sanger DNA sequencing showed no c.3140A > G heterozygous mutation in the PIK3CA gene of this suspected HCC1954 cell line. In addition, we showed the fingerprinting profiles in an unidentified cancer cell line comparison to SiHa cervical cell line, revealing same DNA fingerprinting profiles. In conclusion, we have successfully authenticated and identified both suspected HCC1954 and SiHa cell lines by STR analysis and DNA sequencing. STR analysis combined DNA sequencing may be very useful to evaluate genotypes of cancer cell lines in our cancer studies, as well as in judicial authentication and forensic sciences.

Entities:  

Keywords:  Authentication; Cancer; Cell line; Contamination; Genotype; Quality control; Short-tandem-repeat (STR)

Mesh:

Year:  2018        PMID: 30390187     DOI: 10.1007/s11033-018-4438-7

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  27 in total

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7.  Beware imposters: MA-1, a novel MALT lymphoma cell line, is misidentified and corresponds to Pfeiffer, a diffuse large B-cell lymphoma cell line-A reply: despite the same 8-code STR, MA-1 and Pfeiffer are cytogenetically diverse.

Authors:  Sung-Hsin Kuo; Hui-Jen Tsai; Wen-Hui Weng; Chi-Cheng Li; Kun-Huei Yeh; Li-Tzong Chen; Ann-Lii Cheng
Journal:  Genes Chromosomes Cancer       Date:  2013-11-28       Impact factor: 5.006

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Journal:  Int J Mol Sci       Date:  2018-07-17       Impact factor: 5.923

10.  A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosis.

Authors:  Jiewen Fu; Lu Ma; Jingliang Cheng; Lisha Yang; Chunli Wei; Shangyi Fu; Hongbin Lv; Rui Chen; Junjiang Fu
Journal:  J Cell Mol Med       Date:  2018-08-30       Impact factor: 5.310

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2.  A case of Usher syndrome type IIA caused by a rare USH2A homozygous frameshift variant with maternal uniparental disomy (UPD) in a Chinese family.

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3.  Novel splicing variant c. 208+2T>C in BBS5 segregates with Bardet-Biedl syndrome in an Iranian family by targeted exome sequencing.

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