Evidence map›Paper›PMID 26964624›Full record

ArticleCancer research2016

Cytochrome P450 Allele CYP3A7*1C Associates with Adverse Outcomes in Chronic Lymphocytic Leukemia, Breast, and Lung Cancer.

Nichola Johnson, Paolo De Ieso, Gabriele Migliorini, Nick Orr, Peter Broderick, Daniel Catovsky, Athena Matakidou, Timothy Eisen, Christy Goldsmith, Frank Dudbridge and 6 more

Abstract read
In one paragraph

Article in Cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.0field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Associations Between Cytochrome P450 (CYP) Gene Single-Nucleotide Polymorphisms and Second-to-Fourth Digit Ratio in Chinese University Students.Medical science monitor : international medical journal of experimental and clinical research · 2021
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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

16 authors at 1 institution in 1 country.

Nichola Johnson *Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK and Division of Breast Cancer Research, The Institute of Cancer Research, London, UK.
Paolo De Ieso *Alan Walker Cancer Care Centre, Darwin, Australia.
Gabriele Migliorini *Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
Nick OrrBreast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK and Division of Breast Cancer Research, The Institute of Cancer Research, London, UK.
Peter BroderickDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
Daniel CatovskyDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Athena MatakidouCancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK.
Timothy EisenDepartment of Oncology, Cambridge University Hospitals National Health Service Foundation Trust, Cambridge, UK.
Christy GoldsmithImperial College, London, UK and The Harley Street Clinic, London, UK.
Frank DudbridgeNon-communicable Disease Epidemiology Department, London School of Hygiene and Tropical Medicine, London, UK.
Julian PetoNon-communicable Disease Epidemiology Department, London School of Hygiene and Tropical Medicine, London, UK.
Isabel Dos-Santos-SilvaNon-communicable Disease Epidemiology Department, London School of Hygiene and Tropical Medicine, London, UK.
Alan AshworthBreast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK and Division of Breast Cancer Research, The Institute of Cancer Research, London, UK.
Gillian RossThe Royal Marsden NHS Foundation Trust, Fulham Road, London UK.
Richard S HoulstonDivision of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
Olivia FletcherBreast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK and Division of Breast Cancer Research, The Institute of Cancer Research, London, UK.
The London College · GB

Funding

Breast Cancer Now CTR-Q3FletcherBreast Cancer Now CTR-Q3FLETCHERCancer Research UK 17044Cancer Research UK A5660Cancer Research UK A8362Cancer Research UK A8780Cancer Research UK C1298/A8362Cancer Research UK C1298/A8780Cancer Research UK G1000718Cancer Research UK K006215Medical Research Council G1000718Medical Research Council MR/K006215/1
6 · The paper itself

Abstract

CYP3A enzymes metabolize endogenous hormones and chemotherapeutic agents used to treat cancer, thereby potentially affecting drug effectiveness. Here, we refined the genetic basis underlying the functional effects of a CYP3A haplotype on urinary estrone glucuronide (E1G) levels and tested for an association between CYP3A genotype and outcome in patients with chronic lymphocytic leukemia (CLL), breast, or lung cancers. The most significantly associated SNP was rs45446698, an SNP that tags the CYP3A7*1C allele; this SNP was associated with a 54% decrease in urinary E1G levels. Genotyping this SNP in 1,008 breast cancer, 1,128 lung cancer, and 347 CLL patients, we found that rs45446698 was associated with breast cancer mortality (HR, 1.74; P = 0.03), all-cause mortality in lung cancer patients (HR, 1.43; P = 0.009), and CLL progression (HR, 1.62; P = 0.03). We also found borderline evidence of a statistical interaction between the CYP3A7*1C allele, treatment of patients with a cytotoxic agent that is a CYP3A substrate, and clinical outcome (Pinteraction = 0.06). The CYP3A7*1C allele, which results in adult expression of the fetal CYP3A7 gene, is likely to be the functional allele influencing levels of circulating endogenous sex hormones and outcome in these various malignancies. Further studies confirming these associations and determining the mechanism by which CYP3A7*1C influences outcome are required. One possibility is that standard chemotherapy regimens that include CYP3A substrates may not be optimal for the approximately 8% of cancer patients who are CYP3A7*1C carriers.

Indexed as

AdultAgedAged, 80 and overAllelesAryl Hydrocarbon HydroxylasesBreast NeoplasmsCytochrome P-450 CYP3AEstroneFemaleGenotypeGlucuronidesHumansLeukemia, Lymphocytic, Chronic, B-CellLung NeoplasmsMaleMiddle AgedAryl Hydrocarbon HydroxylasesCYP3A7 protein, humanCytochrome P-450 CYP3AEstroneGlucuronides

Identifiers

PMID26964624
PMCPMC4795533
OpenAlexW2295763822

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.