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Somatic Genetic Variation in Children: from Mosaicism to Cancer

Valind, Anders LU orcid (2017)
Abstract
This thesis concerns various aspects of somatic mosaicism and genetic intratumor heterogeneity in childhood cancer.

In paper I, I show that aneuploidy in itself does not lead to the level of chromosomal instability that is typically seen in malignant cells. This finding strongly argues against the so called autocatalytic theory of carcinogenesis.

Paper II illustrates that, in rare cases, low-level somatic mosaicism can be unmasked by hitchhiking on the clonal expansion seen in carcinogenesis. Paper III demonstrates that the level of somatic mosaicism at the copy number level in fetuses is lower than in adult humans and that fetal hepatocytes are no more aneuploid than other cells from the fetus. Furthermore, we also... (More)
This thesis concerns various aspects of somatic mosaicism and genetic intratumor heterogeneity in childhood cancer.

In paper I, I show that aneuploidy in itself does not lead to the level of chromosomal instability that is typically seen in malignant cells. This finding strongly argues against the so called autocatalytic theory of carcinogenesis.

Paper II illustrates that, in rare cases, low-level somatic mosaicism can be unmasked by hitchhiking on the clonal expansion seen in carcinogenesis. Paper III demonstrates that the level of somatic mosaicism at the copy number level in fetuses is lower than in adult humans and that fetal hepatocytes are no more aneuploid than other cells from the fetus. Furthermore, we also detect an organ specific genomic profile in the fetal thymus, due to physiological T-cell receptor rearrangement.

Paper IV highlights that intratumor genetic heterogeneity is a common feature in chemotherapy treated pediatric cancers. In this paper, we also demonstrate that the presence of genetic heterogeneity within single biopsies is associated with lower event free survival and cancer specific overall survival, and that it was a better prognostic predictor than the burden of somatic genetic aberrations.

Paper V provides a map of the landscape of intratumor genetic heterogeneity within the primary lesion in Wilms tumor, neuroblastoma and rhabdomyosarcoma. We also discover four different evolutionary trajectories, and show that the presence of some of these evolutionary patterns within the primary tumor predicts inferior survival.

In conclusion, the findings presented in this thesis demonstrate that genetic variation is a rare but significant feature in normal cells of young human tissues. In contrast, such variation is extremely common within childhood solid tumors. Our data suggest that increased knowledge of the evolutionary dynamics within a tumor might lead to improved risk stratification and more personalized treatment. (Less)
Please use this url to cite or link to this publication:
author
supervisor
opponent
  • Dr Turajlic, Samra, The Francis Crick Institute and The Royal Marsden Hospital
organization
publishing date
type
Thesis
publication status
published
subject
keywords
Somatic Mosaicism, Cancer, Tumor heterogeneity, Neuroblastoma, Wilms Tumor, Rhabdomyosarcoma, Aneuploidy
pages
58 pages
publisher
Lund University: Faculty of Medicine
defense location
Belfragesalen, BMC D15, Klinikgatan 32 i Lund
defense date
2017-12-15 13:00:00
ISBN
978-91-7619-557-4
language
English
LU publication?
yes
additional info
ISSN: 1652-8220 Lund University, Faculty of Medicine Doctoral Dissertation Series 2017:175
id
7944e59e-f246-44ce-8996-e5f7ed4d1d4d
date added to LUP
2017-11-22 13:55:20
date last changed
2021-03-23 20:04:31
@phdthesis{7944e59e-f246-44ce-8996-e5f7ed4d1d4d,
  abstract     = {{This thesis concerns various aspects of somatic mosaicism and genetic intratumor heterogeneity in childhood cancer.<br/><br/>In paper I, I show that aneuploidy in itself does not lead to the level of chromosomal instability that is typically seen in malignant cells. This finding strongly argues against the so called autocatalytic theory of carcinogenesis.<br/><br/>Paper II illustrates that, in rare cases, low-level somatic mosaicism can be unmasked by hitchhiking on the clonal expansion seen in carcinogenesis. Paper III demonstrates that the level of somatic mosaicism at the copy number level in fetuses is lower than in adult humans and that fetal hepatocytes are no more aneuploid than other cells from the fetus. Furthermore, we also detect an organ specific genomic profile in the fetal thymus, due to physiological T-cell receptor rearrangement.<br/><br/>Paper IV highlights that intratumor genetic heterogeneity is a common feature in chemotherapy treated pediatric cancers. In this paper, we also demonstrate that the presence of genetic heterogeneity within single biopsies is associated with lower event free survival and cancer specific overall survival, and that it was a better prognostic predictor than the burden of somatic genetic aberrations.<br/><br/>Paper V provides a map of the landscape of intratumor genetic heterogeneity within the primary lesion in Wilms tumor, neuroblastoma and rhabdomyosarcoma. We also discover four different evolutionary trajectories, and show that the presence of some of these evolutionary patterns within the primary tumor predicts inferior survival.<br/><br/>In conclusion, the findings presented in this thesis demonstrate that genetic variation is a rare but significant feature in normal cells of young human tissues. In contrast, such variation is extremely common within childhood solid tumors. Our data suggest that increased knowledge of the evolutionary dynamics within a tumor might lead to improved risk stratification and more personalized treatment.}},
  author       = {{Valind, Anders}},
  isbn         = {{978-91-7619-557-4}},
  keywords     = {{Somatic Mosaicism; Cancer; Tumor heterogeneity; Neuroblastoma; Wilms Tumor; Rhabdomyosarcoma; Aneuploidy}},
  language     = {{eng}},
  month        = {{12}},
  publisher    = {{Lund University: Faculty of Medicine}},
  school       = {{Lund University}},
  title        = {{Somatic Genetic Variation in Children: from Mosaicism to Cancer}},
  url          = {{https://lup.lub.lu.se/search/files/35159600/Anders_Valind_WEBB.pdf}},
  year         = {{2017}},
}