Evidence map›Paper›PMID 33194059›Full record

ArticleAmerican journal of translational research2020

Polymorphisms of xenobiotic-metabolizing and transporter genes, and the risk of gastric and colorectal cancer in an admixed population from the Brazilian Amazon.

Amanda Nazaré Cohen Lima de Castro, Marianne Rodrigues Fernandes, Darlen Cardoso de Carvalho, Tatiane Piedade de Souza, Juliana Carla Gomes Rodrigues, Roberta Borges Andrade, Antonio Andre Conde Modesto, Sidney Santos, Paulo Pimentel Assumpção, Ney Pereira Carneiro Dos Santos

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Amanda Nazaré Cohen Lima de CastroOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Marianne Rodrigues FernandesOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Darlen Cardoso de CarvalhoOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Tatiane Piedade de SouzaOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Juliana Carla Gomes RodriguesOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Roberta Borges AndradeOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Antonio Andre Conde ModestoOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Sidney SantosOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Paulo Pimentel AssumpçãoOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Ney Pereira Carneiro Dos SantosOncology Research Center, Universidade Federal do Pará Belém, Brazil.
Universidade Federal do Pará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal (CRC) and gastric (GC) cancers are associated with increased morbidity and mortality. Single nucleotide polymorphisms (SNPs) of xenobiotic metabolism and transporter genes may play a role in the individual responses to exposure to substances implicated in susceptibility to cancer. The investigation of the genetic variation related to the activation and detoxification of xenobiotics may thus help to clarify the prevalence of neoplasms. We analyzed the role of 30 SNPs in xenobiotic-metabolizing and transporter genes in susceptibility to CRC and GC. The study included individuals diagnosed with CRC (n = 121) and GC (n = 95), and 141 controls (non-cancer patients) from the population of Belém, in the Brazilian Amazon. The results indicated an association between the polymorphisms rs2231142 (P = 0.013; OR = 3.01; 95% CI = 1.26-7.13), in the ABCG2 gene, and rs1801159 (P = 0.03; OR = 2.35; 95% CI = 1.14-5.05), in DPYD gene, with the risk of developing GC. The polymorphism rs17116806 of the DPYD gene was found to be associated with a lower risk of developing gastric (P≤0.0001; OR = 0.043; 95% CI = 0.015-0.12) or colorectal (P≤0.0001; OR = 0.076; 95% CI = 0.33-0.18) cancers, indicating that the same variant may play a similar role in different types of cancer tissue. Additionally, the carriers of the TT genotype of the polymorphism in the ABCB1 gene (rs1128503) presented a reduced probability of developing CRC (P = 0.0001; OR = 0.16; 95% CI = 0.06-0.41) as well as GC (P = 0.007; OR = 0.27; 95% CI = 0.1-0.7). Our findings indicate that polymorphisms in xenobiotic-metabolizing and transporter genes may modulate susceptibility to colorectal and gastric cancers.

Indexed as

admixedBrazilcolorectal cancergastric cancerpolymorphismXenobiotics

Identifiers

PMID33194059
PMCPMC7653561
OpenAlexW3100561706

What Socratic holds

Textmetadata
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.