Identification of cancer/testis-antigen genes by massively parallel signature sequencing Journal Article


Authors: Chen, Y. T.; Scanlan, M. J.; Venditti, C. A.; Chua, R.; Theiler, G.; Stevenson, B. J.; Iseli, C.; Gure, A. O.; Vasicek, T.; Strausberg, R. L.; Jongeneel, C. V.; Old, L. J.; Simpson, A. J. G.
Article Title: Identification of cancer/testis-antigen genes by massively parallel signature sequencing
Abstract: Massively parallel signature sequencing (MPSS) generates millions of short sequence tags corresponding to transcripts from a single RNA preparation. Most MPSS tags can be unambiguously assigned to genes, thereby generating a comprehensive expression profile of the tissue of origin. From the comparison of MP55 data from 32 normal human tissues, we identified 1,056 genes that are predominantly expressed in the testis. Further evaluation by using MPSS tags from cancer cell lines and EST data from a wide variety of tumors identified 202 of these genes as candidates for encoding cancer/testis (CT) antigens. Of these genes, the expression in normal tissues was assessed by RT-PCR in a subset of 166 intron-containing genes, and those with confirmed testis-predominant expression were further evaluated for their expression in 21 cancer cell lines. Thus, 20 CT or CT-like genes were identified, with several exhibiting expression in five or more of the cancer cell lines examined. One of these genes is a member of a CT gene family that we designated as CT45. The CT45 family comprises six highly similar (>98% cDNA identity) genes that are clustered in tandem within a 125-kb region on Xq26.3. CT45 was found to be frequently expressed in both cancer cell lines and lung cancer specimens. Thus, MPSS analysis has resulted in a significant extension of our knowledge of CT antigens, leading to the discovery of a distinctive X-linked CT-antigen gene family. © 2005 by The National Academy of Sciences of the USA.
Keywords: controlled study; human tissue; gene sequence; human cell; reverse transcription polymerase chain reaction; gene expression; gene expression profiling; computational biology; intron; lung cancer; genetic transcription; cancer cell culture; cell line, tumor; rna; germ line; molecular sequence data; antigens, neoplasm; reverse transcriptase polymerase chain reaction; rna, messenger; cancer testis antigen; expressed sequence tag; gene identification; nucleotide sequence; base sequence; chromosomes, human, x; dna primers; sequence homology; sequence analysis, rna; testis; expressed sequence tags; normal human; multigene family; dna, complementary; databases, nucleic acid; x chromosome linkage; transcript; chromosome xq
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 102
Issue: 22
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2005-05-31
Start Page: 7940
End Page: 7945
Language: English
DOI: 10.1073/pnas.0502583102
PUBMED: 15905330
PROVIDER: scopus
PMCID: PMC1142383
DOI/URL:
Notes: --- - "Cited By (since 1996): 41" - "Export Date: 24 October 2012" - "CODEN: PNASA" - "Molecular Sequence Numbers: GENBANK: AA884595, AK123209, BC040308, BC047459, BC048128, BC057843, BI818097, BX103208, NM_003323, NM_014269, NM_016585, NM_018666, NM_030812, NM_032037, NM_134444, NM_144613, NM_144979, NM_152582, NM_173493, NM_178173, NM_181502, NM_182791, AY743709, AY743710, AY743711, AY743712, AY743713, AY743714;" - "Source: Scopus"
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MSK Authors
  1. Matthew J Scanlan
    49 Scanlan
  2. Ali O Gure
    29 Gure
  3. Andrew John Simpson
    31 Simpson
  4. Ramon Chua
    21 Chua
  5. Lloyd J Old
    593 Old
  6. Yao-Tseng Chen
    83 Chen
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