LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.

The question of whether "recurrent" laryngeal carcinoma is truly a new tumour with a clonal origin that differs from that of the primary tumour has remained unanswered. The objective of this study was to determine whether recurrent tumours have the same genetic basis as primary tumours, as...

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Main Authors: Zhaoyang Cui, Xinliang Pan, Qirong Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4218824?pdf=render
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spelling doaj-27534d6fc83546dd971057aa5846ddde2020-11-24T21:50:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11185710.1371/journal.pone.0111857LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.Zhaoyang CuiXinliang PanQirong WangThe question of whether "recurrent" laryngeal carcinoma is truly a new tumour with a clonal origin that differs from that of the primary tumour has remained unanswered. The objective of this study was to determine whether recurrent tumours have the same genetic basis as primary tumours, as the answer to this question is important for the development of treatment strategies.Matched samples consisting of primary tumour, recurrent tumour and normal tissue were obtained from the same patient. A total of 37 patients with laryngeal cancer were examined for loss of heterozygosity (LOH) on the 3p, 5p, 7q, 8p, 9p, 13p, 17p and 18q chromosomal arms using PCR to amplify microsatellite markers. All patients were routinely followed up and 5-year survival rates were calculated using directly calculating method and Kaplan-Meier's method.A total of 28 out of 37 (75.6%) patients showed LOH at a minimum of one locus, and 19 out of 37 (51.3%) patients showed LOH at two loci. Primary and recurrent tumours in each patient showed identical allelic loss patterns and incidence rates. Patients without LOH had a longer average time to recurrence than patients with LOH (P<0.05). Additionally, patients with LOH had a longer average smoking duration prior to surgery than patients without LOH (P<0.05). The 5-year survival rates were 32.14%in patients with LOH versus 44.4% in patients without LOH.The data indicate that primary and recurrent tumours have the same clonal origin. This result implies that we failed to radically resect the primary tumours and/or micrometastases in these patients. Consequently, some form of adjunctive therapy may be necessary. Additionally, the data indicate that the recurrence of laryngeal squamous cell carcinoma is closely related to chromosomal aberrations (specifically LOH).http://europepmc.org/articles/PMC4218824?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Zhaoyang Cui
Xinliang Pan
Qirong Wang
spellingShingle Zhaoyang Cui
Xinliang Pan
Qirong Wang
LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
PLoS ONE
author_facet Zhaoyang Cui
Xinliang Pan
Qirong Wang
author_sort Zhaoyang Cui
title LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
title_short LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
title_full LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
title_fullStr LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
title_full_unstemmed LOH detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
title_sort loh detected by microsatellite markers reveals the clonal origin of recurrent laryngeal squamous cell carcinoma.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description The question of whether "recurrent" laryngeal carcinoma is truly a new tumour with a clonal origin that differs from that of the primary tumour has remained unanswered. The objective of this study was to determine whether recurrent tumours have the same genetic basis as primary tumours, as the answer to this question is important for the development of treatment strategies.Matched samples consisting of primary tumour, recurrent tumour and normal tissue were obtained from the same patient. A total of 37 patients with laryngeal cancer were examined for loss of heterozygosity (LOH) on the 3p, 5p, 7q, 8p, 9p, 13p, 17p and 18q chromosomal arms using PCR to amplify microsatellite markers. All patients were routinely followed up and 5-year survival rates were calculated using directly calculating method and Kaplan-Meier's method.A total of 28 out of 37 (75.6%) patients showed LOH at a minimum of one locus, and 19 out of 37 (51.3%) patients showed LOH at two loci. Primary and recurrent tumours in each patient showed identical allelic loss patterns and incidence rates. Patients without LOH had a longer average time to recurrence than patients with LOH (P<0.05). Additionally, patients with LOH had a longer average smoking duration prior to surgery than patients without LOH (P<0.05). The 5-year survival rates were 32.14%in patients with LOH versus 44.4% in patients without LOH.The data indicate that primary and recurrent tumours have the same clonal origin. This result implies that we failed to radically resect the primary tumours and/or micrometastases in these patients. Consequently, some form of adjunctive therapy may be necessary. Additionally, the data indicate that the recurrence of laryngeal squamous cell carcinoma is closely related to chromosomal aberrations (specifically LOH).
url http://europepmc.org/articles/PMC4218824?pdf=render
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AT xinliangpan lohdetectedbymicrosatellitemarkersrevealstheclonaloriginofrecurrentlaryngealsquamouscellcarcinoma
AT qirongwang lohdetectedbymicrosatellitemarkersrevealstheclonaloriginofrecurrentlaryngealsquamouscellcarcinoma
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