Evidence map›Paper›PMID 24950197›Full record

ArticlePloS one2014

Inherited polymorphisms in hyaluronan synthase 1 predict risk of systemic B-cell malignancies but not of breast cancer.

Hemalatha Kuppusamy, Helga M Ogmundsdottir, Eva Baigorri, Amanda Warkentin, Hlif Steingrimsdottir, Vilhelmina Haraldsdottir, Michael J Mant, John Mackey, James B Johnston, Sophia Adamia and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 3 countries.

Hemalatha KuppusamyUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
Helga M OgmundsdottirUniversity of Iceland, Reykjavik, Iceland.
Eva BaigorriUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
Amanda WarkentinUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
Hlif SteingrimsdottirLandspitali University Hospital, Reykjavik, Iceland.
Vilhelmina HaraldsdottirLandspitali University Hospital, Reykjavik, Iceland.
Michael J MantUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
John MackeyUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
James B JohnstonDept. of Hematology, Cancer Care Manitoba and the University of Manitoba, Winnipeg, Manitoba, Canada.
Sophia AdamiaMedical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, United States of America.
Andrew R BelchUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
Linda M PilarskiUniversity of Alberta and Cross Cancer Institute, Edmonton, Alberta, Canada.
University of Alberta · CADana-Farber Cancer Institute · USNational University Hospital of Iceland · ISReykjavík University · ISUniversity of Iceland · ISUniversity of Manitoba · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Genetic variations in the hyaluronan synthase 1 gene (HAS1) influence HAS1 aberrant splicing. HAS1 is aberrantly spliced in malignant cells from multiple myeloma (MM) and Waldenstrom macroglobulinemia (WM), but not in their counterparts from healthy donors. The presence of aberrant HAS1 splice variants predicts for poor survival in multiple myeloma (MM). We evaluated the influence of inherited HAS1 single nucleotide polymorphisms (SNP) on the risk of having a systemic B cell malignancy in 1414 individuals compromising 832 patients and 582 healthy controls, including familial analysis of an Icelandic kindred. We sequenced HAS1 gene segments from 181 patients with MM, 98 with monoclonal gammopathy of undetermined significance (MGUS), 72 with Waldenstrom macroglobulinemia (WM), 169 with chronic lymphocytic leukemia (CLL), as well as 34 members of a monoclonal gammopathy-prone Icelandic family, 212 age-matched healthy donors and a case-control cohort of 295 breast cancer patients with 353 healthy controls. Three linked single nucleotide polymorphisms (SNP) in HAS1 intron3 are significantly associated with B-cell malignancies (range p = 0.007 to p = 10(-5)), but not MGUS or breast cancer, and predict risk in a 34 member Icelandic family (p = 0.005, Odds Ratio = 5.8 (OR)), a relatively homogeneous cohort. In contrast, exon3 SNPs were not significantly different among the study groups. Pooled analyses showed a strong association between the linked HAS1 intron3 SNPs and B-cell malignancies (OR = 1.78), but not for sporadic MGUS or for breast cancer (OR<1.0). The minor allele genotypes of HAS1 SNPs are significantly more frequent in MM, WM, CLL and in affected members of a monoclonal gammopathy-prone family than they are in breast cancer, sporadic MGUS or healthy donors. These inherited changes may increase the risk for systemic B-cell malignancies but not for solid tumors.

Indexed as

AdultAgedAged, 80 and overB-LymphocytesBreast NeoplasmsFemaleGenome-Wide Association StudyGenotypeGlucuronosyltransferaseHumansHyaluronan SynthasesLeukemia, Lymphocytic, Chronic, B-CellMiddle AgedParaproteinemiasPolymorphism, Single NucleotideRisk FactorsGlucuronosyltransferaseHAS1 protein, humanHyaluronan Synthases

Identifiers

PMID24950197
PMCPMC4065063
OpenAlexW1968430784

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.