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Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants
by
Hartmann, Arndt
, Popp, Bernt
, Burghaus, Stefanie
, Agaimy, Abbas
, Erber, Ramona
, Reis, André
, Kraus, Cornelia
, Beckmann, Matthias W.
, Vasileiou, Georgia
, Hoyer, Juliane
in
14/1
/ 14/63
/ 45/22
/ 45/23
/ 45/90
/ 45/91
/ 692/308/2056
/ 692/420/2489/68
/ 692/699/1585/1588/1351
/ 692/699/67/1517
/ 82/51
/ Adult
/ Aged
/ Alleles
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Cancer
/ Cloning
/ Copy number
/ Female
/ Fibroids
/ Fumarase
/ Fumarate Hydratase - genetics
/ Fumarate Hydratase - metabolism
/ Gene frequency
/ Genetic counseling
/ Genomes
/ Germ-Line Mutation
/ Hospitals
/ Humans
/ Kidney cancer
/ Laboratory Medicine
/ Leiomyoma - genetics
/ Leiomyoma - metabolism
/ Leiomyoma - pathology
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Monoclonal antibodies
/ Morphology
/ Mutation
/ Mutation, Missense
/ Oligomerization
/ Pathology
/ Point mutation
/ Renal cell carcinoma
/ Tumors
/ Uterine Neoplasms - genetics
/ Uterine Neoplasms - metabolism
/ Uterine Neoplasms - pathology
/ Uterus
/ Womens health
2020
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Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants
by
Hartmann, Arndt
, Popp, Bernt
, Burghaus, Stefanie
, Agaimy, Abbas
, Erber, Ramona
, Reis, André
, Kraus, Cornelia
, Beckmann, Matthias W.
, Vasileiou, Georgia
, Hoyer, Juliane
in
14/1
/ 14/63
/ 45/22
/ 45/23
/ 45/90
/ 45/91
/ 692/308/2056
/ 692/420/2489/68
/ 692/699/1585/1588/1351
/ 692/699/67/1517
/ 82/51
/ Adult
/ Aged
/ Alleles
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Cancer
/ Cloning
/ Copy number
/ Female
/ Fibroids
/ Fumarase
/ Fumarate Hydratase - genetics
/ Fumarate Hydratase - metabolism
/ Gene frequency
/ Genetic counseling
/ Genomes
/ Germ-Line Mutation
/ Hospitals
/ Humans
/ Kidney cancer
/ Laboratory Medicine
/ Leiomyoma - genetics
/ Leiomyoma - metabolism
/ Leiomyoma - pathology
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Monoclonal antibodies
/ Morphology
/ Mutation
/ Mutation, Missense
/ Oligomerization
/ Pathology
/ Point mutation
/ Renal cell carcinoma
/ Tumors
/ Uterine Neoplasms - genetics
/ Uterine Neoplasms - metabolism
/ Uterine Neoplasms - pathology
/ Uterus
/ Womens health
2020
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Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants
by
Hartmann, Arndt
, Popp, Bernt
, Burghaus, Stefanie
, Agaimy, Abbas
, Erber, Ramona
, Reis, André
, Kraus, Cornelia
, Beckmann, Matthias W.
, Vasileiou, Georgia
, Hoyer, Juliane
in
14/1
/ 14/63
/ 45/22
/ 45/23
/ 45/90
/ 45/91
/ 692/308/2056
/ 692/420/2489/68
/ 692/699/1585/1588/1351
/ 692/699/67/1517
/ 82/51
/ Adult
/ Aged
/ Alleles
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Cancer
/ Cloning
/ Copy number
/ Female
/ Fibroids
/ Fumarase
/ Fumarate Hydratase - genetics
/ Fumarate Hydratase - metabolism
/ Gene frequency
/ Genetic counseling
/ Genomes
/ Germ-Line Mutation
/ Hospitals
/ Humans
/ Kidney cancer
/ Laboratory Medicine
/ Leiomyoma - genetics
/ Leiomyoma - metabolism
/ Leiomyoma - pathology
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Monoclonal antibodies
/ Morphology
/ Mutation
/ Mutation, Missense
/ Oligomerization
/ Pathology
/ Point mutation
/ Renal cell carcinoma
/ Tumors
/ Uterine Neoplasms - genetics
/ Uterine Neoplasms - metabolism
/ Uterine Neoplasms - pathology
/ Uterus
/ Womens health
2020
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Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants
Journal Article
Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants
2020
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Overview
Uterine leiomyomas (ULs) constitute a considerable health burden in the general female population. The fumarate hydratase (FH) deficient subtype is found in up to 1.6% and can occur in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome. We sequenced 13 FH deficient ULs from a previous immunohistochemical screen using a targeted panel and identified biallelic FH variants in all. In eight, we found an FH point mutation (two truncating, six missense) with evidence for loss of the second allele. Variant allele-frequencies in all cases with a point mutation pointed to somatic variants. Spatial clustering of the identified missense variants in the lyase domain indicated altered fumarase oligomerization with subsequent degradation as explanation for the observed FH deficiency. Biallelic FH deletions in five tumors confirm the importance of copy number loss as mutational mechanism. By curating all pathogenic FH variants and calculating their population frequency, we estimate a carrier frequency of up to 1/2,563. Comparing with the prevalence of FH deficient ULs, we conclude that most are sporadic and estimate 2.7–13.9% of females with an FH deficient UL to carry a germline FH variant. Further prospective tumor/normal sequencing studies are needed to develop a reliable screening strategy for HLRCC in women with ULs.
Publisher
Elsevier Inc,Nature Publishing Group US,Elsevier Limited
Subject
/ 14/63
/ 45/22
/ 45/23
/ 45/90
/ 45/91
/ 82/51
/ Adult
/ Aged
/ Alleles
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Cancer
/ Cloning
/ Female
/ Fibroids
/ Fumarase
/ Fumarate Hydratase - genetics
/ Fumarate Hydratase - metabolism
/ Genomes
/ Humans
/ Medicine
/ Mutation
/ Tumors
/ Uterine Neoplasms - genetics
/ Uterine Neoplasms - metabolism
/ Uterine Neoplasms - pathology
/ Uterus
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