Evidence map›Paper›PMID 31218953›Full record

ArticleCurrent pharmaceutical design2019

Effects of As2O3 and Resveratrol on the Proliferation and Apoptosis of Colon Cancer Cells and the hERG-mediated Potential Mechanisms.

Caichuan Yan, Fengmei Li, Yuhao Zhang, Yang Li, Mingzhu Li, Fang Wang, Guocui Zhang, Yuexin Li, Baoxin Li, Xin Zhao

Open access · hybridAbstract read
In one paragraph

Article in Current pharmaceutical design, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 13 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.

Caichuan YanDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Fengmei LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Yuhao ZhangDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Yang LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Mingzhu LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Fang WangDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Guocui ZhangDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Yuexin LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Baoxin LiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Xin ZhaoDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs2O3 and resveratrol have been widely considered to be effective in anti-cancer therapies and the underlying mechanisms have been reported extensively. However, the combined treatment effect and potential target of As2O3 and resveratrol in the treatment of tumors remains elusive. The purpose of this study was to investigate the benefits and efficacy of As2O3 in combination with resveratrol in the treatment of colon cancer, as well as looking for new targets that could provide alternative explanation of the efficacy of drugs.

methodsThe proliferation of cancer cells was measured by the MTT and EdU staining assay, while the apoptosis of cancer cells was determined by the flow cytometry. Western blot and immunoprecipitation were performed to measure the expression levels of proteins and the interaction between hERG and integrin β1, respectively.

resultsIn this study, we found that both As2O3 and resveratrol can effectively inhibit cell proliferation and promote cell apoptosis in colon cancer, and the combined effect of the two drugs on colon cancer cells is more preeminent. The combination of As2O3 with resveratrol, on the one hand reduced the expression of hERG channels on the membrane, and on the other hand weaken the binding between hERG and integrin β 1, which may be the main cause of downstream signaling pathways alterations, including the activation of the apoptotic pathway.

conclusionTaken together, hERG, as a subunit of potassium ion channel on the cell membrane, is highly likely to be involved in the As2O3 and resveratrol induced intracellular signaling cascade disorder, and this novel signaling pathway that sustains the progression of colon cancer may be a promising therapeutic target for human colon cancer treatment in the future.

Indexed as

ApoptosisCell ProliferationAntineoplastic AgentsArsenicalsArsenic TrioxideCell Line, TumorColonic NeoplasmsHumansOxidesResveratrolSignal TransductionTranscriptional Regulator ERGAntineoplastic AgentsArsenicalsArsenic TrioxideERG protein, humanOxidesResveratrolTranscriptional Regulator ERGapoptosiscolon cancerhERGproliferationresveratrolβ1 integrin.

Identifiers

PMID31218953
PMCPMC7040501
OpenAlexW2949738390

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Registered trials

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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.