Evidence map›Paper›PMID 28123853›Full record

ArticleAmerican journal of cancer research2017

Curcumin suppresses epithelial-to-mesenchymal transition and metastasis of pancreatic cancer cells by inhibiting cancer-associated fibroblasts.

Qing Wang, Chao Qu, Fang Xie, Lianyu Chen, Luming Liu, Xiaohua Liang, Xueyong Wu, Peng Wang, Zhiqiang Meng

Open 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. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

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  14. Cancer: a mirrored room between tumor bulk and tumor microenvironment.Journal of experimental & clinical cancer research : CR · 2021
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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

9 authors at 1 institution in 1 country.

Qing WangDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Oncology, Jing'an District Center Hospital of Shanghai (Huashan Hospital, Fudan University, Jing'an Branch)259 Xikang Road, Shanghai 200040, China; Department of Oncology, Huashan Hospital, Fudan University12 Urumqi Road, Shanghai 200040, China.
Chao QuDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Integrative Oncology, Fudan University Shanghai Cancer CenterShanghai, China.
Fang XieDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Oncology, Jing'an District Center Hospital of Shanghai (Huashan Hospital, Fudan University, Jing'an Branch)259 Xikang Road, Shanghai 200040, China.
Lianyu ChenDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Integrative Oncology, Fudan University Shanghai Cancer CenterShanghai, China.
Luming LiuDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Integrative Oncology, Fudan University Shanghai Cancer CenterShanghai, China.
Xiaohua LiangDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Oncology, Huashan Hospital, Fudan University12 Urumqi Road, Shanghai 200040, China.
Xueyong WuDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Oncology, Jing'an District Center Hospital of Shanghai (Huashan Hospital, Fudan University, Jing'an Branch)259 Xikang Road, Shanghai 200040, China.
Peng WangDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Integrative Oncology, Fudan University Shanghai Cancer CenterShanghai, China.
Zhiqiang MengDepartment of Oncology, Shanghai Medical College, Fudan UniversityShanghai, China; Department of Integrative Oncology, Fudan University Shanghai Cancer CenterShanghai, China.
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is one of the most lethal malignancies and the fourth leading cause of cancer-related deaths worldwide, because of its aggressive and highly metastatic ability even in its early stages. Cancer-associated fibroblasts (CAFs) have been reported to be vital to pancreatic cancer progression via regulating tumorigenesis and metastasis. Studies have shown that CAFs also mediate epithelial-to-mesenchymal transition (EMT) in tumor cells. Curcumin has recently been reported to have anticancer effects by modulating pathways involved in cancer progression. Therefore, we hypothesized that curcumin might inhibit EMT by targeting CAFs in pancreatic cancer. In this study, we show that the CAF-mediated enhancement of pancreatic cancer cell migration and metastasis was blocked by curcumin. In conclusion, our data provide the first evidence that curcumin inhibits the migration and metastasis of pancreatic cancer cells by reducing the mesenchymal characteristics of CAFs, which reverses the EMT phenotypes of pancreatic cancer cells.

Indexed as

cancer-associated fibroblasts (CAFs)curcuminepithelial-mesenchymal transition (EMT)metastaticPancreatic cancer

Identifiers

PMID28123853
PMCPMC5250686
OpenAlexW2582912872

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.