Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines

Abstract Background Clonal VDJ rearrangement of B/T cell receptors (B/TCRs) occurring during B/T lymphocyte development has been used as a marker to track the clonality of B/T cell populations. Methods We systematically profiled the B/T cell receptor repertoire of 936 cancer cell lines across a vari...

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Main Authors: Kar-Tong Tan, Ling-Wen Ding, Qiao-Yang Sun, Zhen-Tang Lao, Wenwen Chien, Xi Ren, Jin-Fen Xiao, Xin Yi Loh, Liang Xu, Michael Lill, Anand Mayakonda, De-Chen Lin, Henry Yang, H. Phillip Koeffler
Format: Article
Language:English
Published: BMC 2018-10-01
Series:BMC Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12885-018-4840-5
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author Kar-Tong Tan
Ling-Wen Ding
Qiao-Yang Sun
Zhen-Tang Lao
Wenwen Chien
Xi Ren
Jin-Fen Xiao
Xin Yi Loh
Liang Xu
Michael Lill
Anand Mayakonda
De-Chen Lin
Henry Yang
H. Phillip Koeffler
author_facet Kar-Tong Tan
Ling-Wen Ding
Qiao-Yang Sun
Zhen-Tang Lao
Wenwen Chien
Xi Ren
Jin-Fen Xiao
Xin Yi Loh
Liang Xu
Michael Lill
Anand Mayakonda
De-Chen Lin
Henry Yang
H. Phillip Koeffler
author_sort Kar-Tong Tan
collection DOAJ
description Abstract Background Clonal VDJ rearrangement of B/T cell receptors (B/TCRs) occurring during B/T lymphocyte development has been used as a marker to track the clonality of B/T cell populations. Methods We systematically profiled the B/T cell receptor repertoire of 936 cancer cell lines across a variety of cancer types as well as 462 Epstein-Barr Virus (EBV) transformed normal B lymphocyte lines using RNA sequencing data. Results Rearranged B/TCRs were readily detected in cell lines derived from lymphocytes, and subclonality or potential biclonality were found in a number of blood cancer cell lines. Clonal BCR/TCR rearrangements were detected in several blast phase CML lines and unexpectedly, one gastric cancer cell line (KE-97), reflecting a lymphoid origin of these cells. Notably, clonality was highly prevalent in EBV transformed B lymphocytes, suggesting either transformation only occurred in a few B cells or those with a growth advantage dominated the transformed population through clonal evolution. Conclusions Our analysis reveals the complexity and heterogeneity of the BCR/TCR rearrangement repertoire and provides a unique insight into the clonality of lymphocyte derived cell lines.
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spelling doaj.art-ab73d11ede72491d9a1d5693f9503c262022-12-21T19:16:21ZengBMCBMC Cancer1471-24072018-10-0118111310.1186/s12885-018-4840-5Profiling the B/T cell receptor repertoire of lymphocyte derived cell linesKar-Tong Tan0Ling-Wen Ding1Qiao-Yang Sun2Zhen-Tang Lao3Wenwen Chien4Xi Ren5Jin-Fen Xiao6Xin Yi Loh7Liang Xu8Michael Lill9Anand Mayakonda10De-Chen Lin11Henry Yang12H. Phillip Koeffler13Cancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeDivision of Hematology/Oncology, Cedars-Sinai Medical Center, UCLA School of MedicineCancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeDivision of Hematology/Oncology, Cedars-Sinai Medical Center, UCLA School of MedicineCancer Science Institute of Singapore, National University of SingaporeDivision of Hematology/Oncology, Cedars-Sinai Medical Center, UCLA School of MedicineCancer Science Institute of Singapore, National University of SingaporeCancer Science Institute of Singapore, National University of SingaporeAbstract Background Clonal VDJ rearrangement of B/T cell receptors (B/TCRs) occurring during B/T lymphocyte development has been used as a marker to track the clonality of B/T cell populations. Methods We systematically profiled the B/T cell receptor repertoire of 936 cancer cell lines across a variety of cancer types as well as 462 Epstein-Barr Virus (EBV) transformed normal B lymphocyte lines using RNA sequencing data. Results Rearranged B/TCRs were readily detected in cell lines derived from lymphocytes, and subclonality or potential biclonality were found in a number of blood cancer cell lines. Clonal BCR/TCR rearrangements were detected in several blast phase CML lines and unexpectedly, one gastric cancer cell line (KE-97), reflecting a lymphoid origin of these cells. Notably, clonality was highly prevalent in EBV transformed B lymphocytes, suggesting either transformation only occurred in a few B cells or those with a growth advantage dominated the transformed population through clonal evolution. Conclusions Our analysis reveals the complexity and heterogeneity of the BCR/TCR rearrangement repertoire and provides a unique insight into the clonality of lymphocyte derived cell lines.http://link.springer.com/article/10.1186/s12885-018-4840-5BCR/TCR receptor repertoireEBV lymphocytesCancer cell lines
spellingShingle Kar-Tong Tan
Ling-Wen Ding
Qiao-Yang Sun
Zhen-Tang Lao
Wenwen Chien
Xi Ren
Jin-Fen Xiao
Xin Yi Loh
Liang Xu
Michael Lill
Anand Mayakonda
De-Chen Lin
Henry Yang
H. Phillip Koeffler
Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines
BMC Cancer
BCR/TCR receptor repertoire
EBV lymphocytes
Cancer cell lines
title Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines
title_full Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines
title_fullStr Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines
title_full_unstemmed Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines
title_short Profiling the B/T cell receptor repertoire of lymphocyte derived cell lines
title_sort profiling the b t cell receptor repertoire of lymphocyte derived cell lines
topic BCR/TCR receptor repertoire
EBV lymphocytes
Cancer cell lines
url http://link.springer.com/article/10.1186/s12885-018-4840-5
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