Evidence map›Paper›PMID 28337376›Full record

ArticleAmerican journal of cancer research2017

Curcumin derivative WZ35 efficiently suppresses colon cancer progression through inducing ROS production and ER stress-dependent apoptosis.

Junru Zhang, Zhiguo Feng, Chunhua Wang, Huiping Zhou, Weidong Liu, Karvannan Kanchana, Xuanxuan Dai, Peng Zou, Junlian Gu, Lu Cai and 1 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 59 citations in OpenAlex.

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  11. Updated Review on the Role of Curcumin in Gastrointestinal Cancers.Advances in experimental medicine and biology · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Junru ZhangChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical UniversityWenzhou, Zhejiang 325035, China; Chinese-American Research Institute for Diabetic Complications, School of Pharmaceutical Science, Wenzhou Medical UniversityWenzhou, Zhejiang 325035, China; School of Pharmaceutical Science, Binzhou Medical UniversityYantai, Shandong 264003, China.
Zhiguo FengChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Chunhua WangSchool of Pharmaceutical Science, Binzhou Medical University Yantai, Shandong 264003, China.
Huiping ZhouChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Weidong LiuChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Karvannan KanchanaChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Xuanxuan DaiChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Peng ZouChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Junlian GuChinese-American Research Institute for Diabetic Complications, School of Pharmaceutical Science, Wenzhou Medical UniversityWenzhou, Zhejiang 325035, China; Kosair Children's Hospital Research Institute, Department of Pediatrics of The University of LouisvilleLouisville, KY 40202, USA.
Lu CaiChinese-American Research Institute for Diabetic Complications, School of Pharmaceutical Science, Wenzhou Medical UniversityWenzhou, Zhejiang 325035, China; Kosair Children's Hospital Research Institute, Department of Pediatrics of The University of LouisvilleLouisville, KY 40202, USA.
Guang LiangChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University Wenzhou, Zhejiang 325035, China.
Wenzhou Medical University · CNBoston Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colon cancer is characterized by its fast progression and poor prognosis, and novel agents of treating colon cancer are urgently needed. WZ35, a synthetic curcumin derivative, has been reported to exhibit promising antitumor activity. Here, we investigated the in vitro and in vivo activities of WZ35 and explored the underlying mechanisms in colon cancer cell lines. WZ35 treatment significantly decreased the cell viability associated with G2/M cell cycle arrest and apoptosis induction in colon cancer cell lines. We also show that WZ35 is highly effective in inhibiting tumor growth in a CT26 xenograft mouse model. Mechanistically, WZ35 treatment significantly induced reactive oxygen species (ROS) generation and endoplasmic reticulum (ER) stress in CT26 cells. Abrogation of ROS production by N-acetylcysteine (NAC) co-treatment almost totally reversed the WZ35-induced cell apoptosis and ER stress activation. Inhibition of p-PERK by GSK2606414 can significantly reverse WZ35-induced cell apoptosis in CT26 cells. Taken together, the curcumin derivative WZ35 exhibited anti-tumor effects in colon cancer cells both in vitro and in vivo, via a ROS-ER stress-mediated mechanism. These findings indicate that activating ROS generation could be an important strategy for the treatment of colon cancers.

Indexed as

apoptosisColon cancercurcumin derivativeendoplasmic reticulum stressreactive oxygen species

Identifiers

PMID28337376
PMCPMC5336501
OpenAlexW2980427346

What OpenQuestion 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 OpenQuestion graph.