Evidence map›Paper›PMID 35408903›Full record

ArticleInternational journal of molecular sciences2022

Kaempferol Can Reverse the 5-Fu Resistance of Colorectal Cancer Cells by Inhibiting PKM2-Mediated Glycolysis.

Haili Wu, Jin'e Du, Chenglu Li, Hanqing Li, Huiqin Guo, Zhuoyu Li

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 94 citations in OpenAlex.

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  9. 3,3'-Di-O-methylellagic Acid Isolated fromPharmaceuticals (Basel, Switzerland) · 2026
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12 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Haili WuCollege of Life Science, Shanxi University, Taiyuan 030006, China.
Jin'e DuCollege of Life Science, Shanxi University, Taiyuan 030006, China.
Chenglu LiCollege of Life Science, Shanxi University, Taiyuan 030006, China.
Hanqing LiCollege of Life Science, Shanxi University, Taiyuan 030006, China.
Huiqin GuoThe Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Biotechnology, Shanxi University, Taiyuan 030006, China.
Zhuoyu LiThe Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Biotechnology, Shanxi University, Taiyuan 030006, China.
Shanxi University · CN

Funding

National Natural Science Foundation of China 31770382National Natural Science Foundation of China 31800290National Natural Science Foundation of China 82072718Project of the Central Government Guiding Local Science and Technology YDZX20201400001436Science and Technology Innovation Project of Colleges and Universities in Shanxi Province 2019L0027
6 · The paper itself

Abstract

Resistance to 5-Fluorouracil (5-Fu) chemotherapy is the main cause of treatment failure in the cure of colon cancer. Therefore, there is an urgent need to explore a safe and effective multidrug resistance reversal agent for colorectal cancer, which would be of great significance for improving clinical efficacy. The dietary flavonoid kaempferol plays a key role in the progression of colorectal cancer and 5-Fu resistance. However, the molecular mechanism of kaempferol in reversing 5-Fu resistance in human colorectal cancer cells is still unclear. We found that kaempferol could reverse the drug resistance of HCT8-R cells to 5-Fu, suggesting that kaempferol alone or in combination with 5-Fu has the potential to treat colorectal cancer. It is well known that aerobic glycolysis is related to tumor growth and chemotherapy resistance. Indeed, kaempferol treatment significantly reduced glucose uptake and lactic acid production in drug-resistant colorectal cancer cells. In terms of mechanism, kaempferol promotes the expression of microRNA-326 (miR-326) in colon cancer cells, and miR-326 could inhibit the process of glycolysis by directly targeting pyruvate kinase M2 isoform (PKM2) 3'-UTR (untranslated region) to inhibit the expression of PKM2 or indirectly block the alternative splicing factors of PKM mRNA, and then reverse the resistance of colorectal cancer cells to 5-Fu. Taken together, our data suggest that kaempferol may play an important role in overcoming resistance to 5-Fu therapy by regulating the miR-326-hnRNPA1/A2/PTBP1-PKM2 axis.

Indexed as

Colonic NeoplasmsColorectal NeoplasmsMicroRNAsCarrier ProteinsCell Line, TumorDrug Resistance, NeoplasmFluorouracilGene Expression Regulation, NeoplasticGlycolysisHeterogeneous-Nuclear RibonucleoproteinsHumansKaempferolsMembrane ProteinsPolypyrimidine Tract-Binding ProteinThyroid Hormone-Binding ProteinsThyroid HormonesCarrier ProteinsFluorouracilHeterogeneous-Nuclear RibonucleoproteinskaempferolKaempferolsMembrane ProteinsMicroRNAsMIRN326 microRNA, humanPolypyrimidine Tract-Binding ProteinPTBP1 protein, humanThyroid Hormone-Binding ProteinsThyroid Hormones5-Fu resistanceaerobic glycolysiscolorectal cancerkaempferolmiR-326PKM2

Identifiers

PMID35408903
PMCPMC8998549
OpenAlexW4220702628

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.