MétaCan
Menu
Back to cohort
Record W4298328825 · doi:10.17615/v5y9-k642

Variants in autophagy-related genes and clinical characteristics in melanoma: a population-based study

2020· article· en· W4298328825 on OpenAlexfundno aff
Roberto Zanetti, Melisa Litchfield, Urvi Mujumdar, Paul Tucker, Klaus J. Busam, Lynn From, Terence Dwyer, Elizabeth Theis, Irene Orlow, Nicola Stephens, Joanne Jeter, Anne Kricker, Stefano Rosso, Dianne Mattingly, Lidia Sacchetto, Noori Chowdhury, Loraine D. Marrett, Nancy Leighton, Li Luo, Hoda Anton‐Culver, Amy V. Walker, Alison Venn, Peter A. Kanetsky, Kirsten A. White, Pampa Roy, Timothy R. Rebbeck, Homer Wilcox, Todd A. Thompson, Louise Vanasse, Nancy E. Thomas, Judith B. Klotz, Colin B. Begg, Anne Ε. Cust, Jon Player, Carlotta Sacerdote, Saarene Panossian, Marianne Berwick, Teresa Switzer, Jenna Lilyquist, S. Madronich, Stephen B. Gruber, Chien‐An Andy Hu, Salina Torres, Richard P. Gallagher, Bruce K. Armstrong, Julia Lee Taylor, Helen A. Weiss

Bibliographic record

VenueUNC Libraries · 2020
Typearticle
Languageen
FieldMedicine
TopicAutophagy in Disease and Therapy
Canadian institutionsnot available
FundersBC Cancer AgencyUniversity of California, IrvineNational Cancer InstituteUniversity of North Carolina at Chapel HillNational Institutes of HealthMenzies Institute for Medical ResearchCancer Care OntarioMissouri Department of Health and Senior ServicesUniversity of TasmaniaUniversity of PennsylvaniaState of New Jersey Department of Health
KeywordsAutophagyGeneMelanomaGeneticsBiologyPopulationComputational biologyMedicineEnvironmental health

Abstract

fetched live from OpenAlex

Autophagy has been linked with melanoma risk and survival, but no polymorphisms in autophagy-related (ATG) genes have been investigated in relation to melanoma progression. We examined five single-nucleotide polymorphisms (SNPs) in three ATG genes (ATG5; ATG10; and ATG16L) with known or suspected impact on autophagic flux in an international population-based case-control study of melanoma. DNA from 911 melanoma patients was genotyped. An association was identified between (GG) (rs2241880) and earlier stage at diagnosis (OR 0.47; 95% Confidence Intervals (CI) = 0.27-0.81, P = 0.02) and a decrease in Breslow thickness (P = 0.03). The ATG16L heterozygous genotype (AG) (rs2241880) was associated with younger age at diagnosis (P = 0.02). Two SNPs in ATG5 were found to be associated with increased stage (rs2245214 CG, OR 1.47; 95% CI = 1.11-1.94, P = 0.03; rs510432 CC, OR 1.84; 95% CI = 1.12-3.02, P = 0.05). Finally, we identified inverse associations between ATG5 (GG rs2245214) and melanomas on the scalp or neck (OR 0.20, 95% CI = 0.05-0.86, P = 0.03); ATG10 (CC) (rs1864182) and brisk tumor infiltrating lymphocytes (TILs) (OR 0.42; 95% CI = 0.21-0.88, P = 0.02), and ATG5 (CC) (rs510432) with nonbrisk TILs (OR 0.55; 95% CI = 0.34-0.87, P = 0.01). Our data suggest that ATG SNPs might be differentially associated with specific host and tumor characteristics including age at diagnosis, TILs, and stage. These associations may be critical to understanding the role of autophagy in cancer, and further investigation will help characterize the contribution of these variants to melanoma progression.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.030
GPT teacher head0.297
Teacher spread0.267 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2020
Admission routes1
Has abstractyes

Explore more

Same venueUNC LibrariesSame topicAutophagy in Disease and TherapyFrench-language works237,207