Evidence map›Paper›PMID 28402965›Full record

ArticleOncotarget2017

Curcumin enhances the effects of irinotecan on colorectal cancer cells through the generation of reactive oxygen species and activation of the endoplasmic reticulum stress pathway.

Yan-Feng Huang, Da-Jian Zhu, Xiao-Wu Chen, Qi-Kang Chen, Zhen-Tao Luo, Chang-Chun Liu, Guo-Xin Wang, Wei-Jie Zhang, Nv-Zhu Liao

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 96 citations in OpenAlex.

  1. IGFBP-3 enhances irinotecan efficacy in colorectal cancerResearch in pharmaceutical sciences · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Article
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 3 institutions in 1 country.

Yan-Feng HuangDepartment of Traditional Chinese Medicine, Shunde Hospital of Southern Medical University, Guangdong 528300, China.
Da-Jian ZhuDepartment of Gastrointestinal Surgery, Shunde Women and Children's Hospital Affiliated to Jinan University, Guangdong 528300, China.
Xiao-Wu ChenDepartment of Gastrointestinal Surgery, Shunde Hospital of Southern Medical University, Guangdong 528300, China.
Qi-Kang ChenDepartment of Gastrointestinal Surgery, Shunde Women and Children's Hospital Affiliated to Jinan University, Guangdong 528300, China.
Zhen-Tao LuoDepartment of Gastrointestinal Surgery, Shunde Hospital of Southern Medical University, Guangdong 528300, China.
Chang-Chun LiuDepartment of Gastrointestinal Surgery, Shunde Hospital of Southern Medical University, Guangdong 528300, China.
Guo-Xin WangDepartment of Gastrointestinal Surgery, Shunde Hospital of Southern Medical University, Guangdong 528300, China.
Wei-Jie ZhangDepartment of Gastrointestinal Surgery, Shunde Hospital of Southern Medical University, Guangdong 528300, China.
Nv-Zhu LiaoDepartment of Gastrointestinal Surgery, Shunde Women and Children's Hospital Affiliated to Jinan University, Guangdong 528300, China.
Jinan University · CNSouthern Medical University · CNThe First People's Hospital of Shunde · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although initially effective against metastatic colorectal cancer (CRC), irinotecan-based chemotherapy leads to resistance and adverse toxicity. Curcumin is well known for its anti-cancer effects in many cancers, including CRC. Here, we describe reactive oxygen species (ROS) generation and endoplasmic reticulum (ER) stress as important mechanisms by which curcumin enhances irinotecan's effects on CRC cells. CRC cell lines were treated with curcumin and/or irinotecan for 24 h, and then evaluated using cell proliferation assays, cell apoptosis assays, cell cycle analysis, intracellular Ca2+ measurements, ROS measurements and immunoblotting for key ER stress-related proteins. We found that cell viability was inhibited and apoptosis was increased, accompanied by ROS generation and ER stress activation in CRC cells treated with curcumin alone or in combination with irinotecan. Blocking ROS production attenuated the expression of two markers of ER stress: binding of immunoglobulin protein (BIP) and CCAAT/enhancer-binding protein homologous protein (CHOP). Blocking CHOP expression using RNA interference also inhibited ROS generation. These results demonstrated that curcumin could enhance the effects of irinotecan on CRC cells by inhibiting cell viability and inducing cell cycle arrest and apoptosis, and that these effects may be mediated, in part, by ROS generation and activation of the ER stress pathway.

Indexed as

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCalciumCamptothecinCell Cycle CheckpointsCell Line, TumorCell ProliferationCell SurvivalColonic NeoplasmsCurcuminDrug SynergismDrug Therapy, CombinationEndoplasmic Reticulum Chaperone BiPEndoplasmic Reticulum StressHeat-Shock ProteinsAntineoplastic AgentsCalciumCamptothecinCurcuminDDIT3 protein, humanEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsIrinotecanReactive Oxygen SpeciesRNA, Small InterferingTranscription Factor CHOPcolorectal cancercurcuminER stressirinotecanROS

Identifiers

PMID28402965
PMCPMC5522238
OpenAlexW2604490519

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.