A pan-cancer landscape of telomeric content shows that RAD21 and HGF alterations are associated with longer telomeres
Background Cancer cells can proliferate indefinitely through telomere maintenance mechanisms. These mechanisms include telomerase-dependent elongation, mediated by TERT activation, and alternative lengthening of telomeres (ALT), linked to loss of ATRX or DAXX . Methods We analyzed the telomeric cont...
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Published in | Genome medicine Vol. 14; no. 1; pp. 25 - 15 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
26.02.2022
BioMed Central Ltd BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1756-994X 1756-994X |
DOI | 10.1186/s13073-022-01029-7 |
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Summary: | Background
Cancer cells can proliferate indefinitely through telomere maintenance mechanisms. These mechanisms include telomerase-dependent elongation, mediated by
TERT
activation, and alternative lengthening of telomeres (ALT), linked to loss of
ATRX
or
DAXX
.
Methods
We analyzed the telomeric content of 89,959 tumor samples within the Foundation Medicine dataset and investigated the genomic determinants of high telomeric content, linking them to clinical outcomes, when available.
Results
Telomeric content varied widely by disease type with leiomyosarcoma having the highest and Merkel cell carcinoma having the lowest telomeric content. In agreement with previous studies, telomeric content was significantly higher in samples with alterations in
TERC
,
ATRX,
and
DAXX
. We further identified that amplifications in two genes,
RAD21
and
HGF
, were enriched in samples with high telomeric content, which was confirmed using the PCAWG/ICGC dataset. We identified the minimal amplified region associated with high telomeric content for
RAD21
(8q23.1–8q24.12), which excludes
MYC
, and for
HGF
(7q21.11). Our results demonstrated that
RAD21
and
HGF
exerted an additive telomere lengthening effect on samples with existing alterations in canonical genes previously associated with telomere elongation. Furthermore, patients with breast cancer who harbor
RAD21
alterations had poor median overall survival and trended towards higher levels of Ki-67 staining.
Conclusions
This study highlights the importance of the role played by
RAD21
(8q23.1–8q24.12) and
HGF
(7q21.11) in the lengthening of telomeres, supporting unlimited replication in tumors. These findings open avenues for work aimed at targeting this crucial pathway in tumorigenesis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1756-994X 1756-994X |
DOI: | 10.1186/s13073-022-01029-7 |