Evidence map›Paper›PMID 25108739›Full record

ArticleBreast cancer research and treatment2014

Association between germline single nucleotide polymorphisms in the PI3K-AKT-mTOR pathway, obesity, and breast cancer disease-free survival.

Mala Pande, Melissa L Bondy, Kim-Anh Do, Aysegul A Sahin, Jun Ying, Gordon B Mills, Patricia A Thompson, Abenaa M Brewster

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  15. Luteolin induces apoptosisOncology letters · 2017
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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

8 authors at 3 institutions in 1 country.

Mala PandeDepartment of Gastroenterology - Research, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Melissa L Bondy
Kim-Anh Do
Aysegul A Sahin
Jun Ying
Gordon B Mills
Patricia A Thompson
Abenaa M Brewster
The University of Texas MD Anderson Cancer Center · USChildren's Cancer Center · USUniversity of Arizona Cancer Center

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UTMDACC SPORE in Breast CancerP50CA116199 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BERRY, DONALD A · 2005 to 2009
$11.9M
Risk Prediction for ER Negative Breast Cancer RecurrenceR01CA172511 · NCI · BAYLOR COLLEGE OF MEDICINE · PI BONDY, MELISSA L., BREWSTER, ABENAA M · 2013 to 2017
$3.1M
Determinants of Breast Cancer SurvivalR01CA089608 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BONDY, MELISSA L · 2002 to 2006
$3.1M
Susceptibility Markers for a Breast-Colon Cancer PhenotypeK07CA160753 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI PANDE, MALA · 2012 to 2016
$603k
NCI NIH HHS K07 CA160753NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA116199NCI NIH HHS P50CA116199NCI NIH HHS R01 CA089608NCI NIH HHS R01 CA172511
6 · The paper itself

Abstract

Obesity-related hormones and cytokines alter PI3 K-AKT-mTOR pathway activation in breast tumors contributing to poorer disease-free survival (DFS) and decreased responsiveness to tamoxifen and trastuzumab. We hypothesized that single nucleotide polymorphisms (SNPs) in candidate genes in the PI3 K-AKT-mTOR signaling pathway may act as genetic modifiers of breast cancer DFS. We analyzed the association of 106 tagging SNPs in 13 genes (ADIPOQ, IGF1, INS, IRS1, LEP, LEPR, LEPROT, PIK3CA, PIK3R5, PTEN, TSC1, TSC2, and AKT1) in the P13K-AKT-mTOR pathway with DFS in a sample of 1,019 women with stage I-II breast cancer. SNPs significantly associated with DFS in any genetic model (additive, dominant, or recessive) after correcting for false discovery rate (FDR = 0.10) were included in Cox proportional hazards multivariable analyses. After adjusting for race/ethnicity, age at diagnosis, tumor stage, and treatment, rs1063539 in ADIPOQ, rs11585329 in LEPR, and rs2519757 in TSC1 were associated with improved DFS, and rs1520220 in IGF1 and rs2677760 in PIK3CA were associated with worse DFS. The associations were not significantly modified by the type of systemic treatment received or body mass index. The SNPs were not associated with tumor characteristics such as tumor size, lymph node status, nuclear grade, or hormone receptor status. In this study, germline SNPs in the PI3 K-AKT-mTOR pathway were associated with breast cancer DFS and may be potential prognostic markers. Future studies are needed to replicate our results and to evaluate the relationship between these polymorphisms and activation of the PI3 K-AKT-mTOR pathway in breast tumors.

Indexed as

Breast NeoplasmsDisease-Free SurvivalFemaleGenetic Predisposition to DiseaseHumansMiddle AgedNeoplasm StagingObesityPhosphatidylinositol 3-KinasesPolymorphism, Single NucleotideProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID25108739
PMCPMC4174407
OpenAlexW1995575450

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.