Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers

This study attempts to determine whether primary tumor tissue could reliably represent metastatic colorectal cancer in therapy-guiding analysis of mitochondrial microsatellite instability. Therefore, we investigated the concordance of microsatellite instability in D310, D514, and D16184 (mitochondri...

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Main Authors: Britta Kleist, Thuja Meurer, Micaela Poetsch
Format: Article
Language:English
Published: IOS Press 2017-03-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317692246
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spelling doaj-8351f9c8dc134af78f4d5cc1023bda9c2021-05-02T18:10:10ZengIOS PressTumor Biology1423-03802017-03-013910.1177/1010428317692246Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markersBritta Kleist0Thuja Meurer1Micaela Poetsch2Department of Pathology, Southern Hospital Trust, Kristiansand, NorwayInstitute of Legal Medicine, University Hospital Essen, Essen, GermanyInstitute of Legal Medicine, University Hospital Essen, Essen, GermanyThis study attempts to determine whether primary tumor tissue could reliably represent metastatic colorectal cancer in therapy-guiding analysis of mitochondrial microsatellite instability. Therefore, we investigated the concordance of microsatellite instability in D310, D514, and D16184 (mitochondrial DNA displacement loop), and its association with selected clinical categories and KRAS/NRAS/BRAF/PIK3CA/TP53 mutation status between primary and metastatic colorectal cancer tissue from 119 patients. Displacement loop microsatellite instability was significantly more frequently seen in lymph node metastases (53.1%) compared to primary tumors (37.5%) and distant metastases (21.4%) ( p  = 0.0183 and p  = 0.0005). The discordant rate was significantly higher in lymph node metastases/primary tumor pairs (74.6%) than in distant metastases/primary tumor pairs (52.4%) or lymph node metastases/distant metastases pairs (51.6%) ( p  = 0.0113 and p  = 0.0261) with more gain (86.7%) than loss (61.1%) of microsatellite instability in the discordant lymph node metastases ( p  = 0.0024). Displacement loop instability occurred significantly more frequently in lymph node metastases and distant metastases of patients with early colorectal cancer onset age <60 years ( p  = 0.0122 and p  = 0.0129), was found with a significant high rate in a small cohort of TP53 -mutated distant metastases ( p  = 0.0418), and was associated with TP53 wild-type status of primary tumors ( p  = 0.0009), but did not correlate with KRAS , NRAS , BRAF , or PIK3CA mutations. In conclusion, mitochondrial microsatellite instability and its association with selected clinical and molecular markers are discordant in primary and metastatic colorectal cancer, which could have importance for surveillance and therapeutic strategies.https://doi.org/10.1177/1010428317692246
collection DOAJ
language English
format Article
sources DOAJ
author Britta Kleist
Thuja Meurer
Micaela Poetsch
spellingShingle Britta Kleist
Thuja Meurer
Micaela Poetsch
Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers
Tumor Biology
author_facet Britta Kleist
Thuja Meurer
Micaela Poetsch
author_sort Britta Kleist
title Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers
title_short Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers
title_full Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers
title_fullStr Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers
title_full_unstemmed Mitochondrial DNA alteration in primary and metastatic colorectal cancer: Different frequency and association with selected clinicopathological and molecular markers
title_sort mitochondrial dna alteration in primary and metastatic colorectal cancer: different frequency and association with selected clinicopathological and molecular markers
publisher IOS Press
series Tumor Biology
issn 1423-0380
publishDate 2017-03-01
description This study attempts to determine whether primary tumor tissue could reliably represent metastatic colorectal cancer in therapy-guiding analysis of mitochondrial microsatellite instability. Therefore, we investigated the concordance of microsatellite instability in D310, D514, and D16184 (mitochondrial DNA displacement loop), and its association with selected clinical categories and KRAS/NRAS/BRAF/PIK3CA/TP53 mutation status between primary and metastatic colorectal cancer tissue from 119 patients. Displacement loop microsatellite instability was significantly more frequently seen in lymph node metastases (53.1%) compared to primary tumors (37.5%) and distant metastases (21.4%) ( p  = 0.0183 and p  = 0.0005). The discordant rate was significantly higher in lymph node metastases/primary tumor pairs (74.6%) than in distant metastases/primary tumor pairs (52.4%) or lymph node metastases/distant metastases pairs (51.6%) ( p  = 0.0113 and p  = 0.0261) with more gain (86.7%) than loss (61.1%) of microsatellite instability in the discordant lymph node metastases ( p  = 0.0024). Displacement loop instability occurred significantly more frequently in lymph node metastases and distant metastases of patients with early colorectal cancer onset age <60 years ( p  = 0.0122 and p  = 0.0129), was found with a significant high rate in a small cohort of TP53 -mutated distant metastases ( p  = 0.0418), and was associated with TP53 wild-type status of primary tumors ( p  = 0.0009), but did not correlate with KRAS , NRAS , BRAF , or PIK3CA mutations. In conclusion, mitochondrial microsatellite instability and its association with selected clinical and molecular markers are discordant in primary and metastatic colorectal cancer, which could have importance for surveillance and therapeutic strategies.
url https://doi.org/10.1177/1010428317692246
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