Evidence map›Paper›PMID 38256877›Full record

ArticlePharmaceuticals (Basel, Switzerland)2023

Isoliquiritigenin Inhibits the Growth of Colorectal Cancer Cells through the ESR2/PI3K/AKT Signalling Pathway.

Fenglin Luo, Yimeng Tang, Lin Zheng, Ying Yang, Haoyue Gao, Shiya Tian, Hongyu Chen, Chenxi Tang, Shanshan Tang, Qiong Man and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. 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

11 authors at 1 institution in 1 country.

Fenglin LuoDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Yimeng TangDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Lin ZhengDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Ying YangDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Haoyue GaoDepartment of Geriatrics, Women and Children, School of Nursing, Chengdu Medical College, Chengdu 610106, China.
Shiya TianDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Hongyu ChenDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Chenxi TangDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Shanshan TangDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Qiong ManDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Yiying WuDepartment of Pharmacology, School of Pharmacy, Chengdu Medical College, Chengdu 610500, China.
Chengdu Medical College · CN

Funding

National College Students' innovation and entrepreneurship training program 202213705023National College Students' innovation and entrepreneurship training program 202313705032Natural Science Foundation of Science and Technology Department of Sichuan Province 2022NSFSC1440Sichuan Province College Students' Innovation and Entrepreneurship Training Program S202313705080
6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most common malignancies. Isoliquiritigenin (ISL), a flavonoid phytoestrogen, has shown anti-tumour activities against various cancers. However, its anti-CRC mechanism has not been clarified. In this study, the potential molecular mechanism of ISL against CRC was investigated through network pharmacological prediction and experimental validation. The results of the network prediction indicate that ESR2, PIK3CG and GSK3β might be the key targets of ISL against CRC, which was verified by molecular docking, and that its anti-tumour mechanisms might be related to the oestrogen and PI3K/AKT signalling pathway. The experimental results show that ISL reduced the viability of SW480 and HCT116 cells, induced apoptosis, blocked the cell cycle in the G2 phase in vitro, and suppressed xenograft tumour growth in vivo. In addition, ISL significantly down-regulated the protein expression of PIK3CG, AKT, p-AKT, p-GSK3β, CDK1, NF-κB and Bcl-2; up-regulated ESR2 and Bax; decreased the ratio of p-AKT/AKT and p-GSK3β/GSK3β; and increased the Bax/Bcl-2 ratio. This study indicates that ISL can inhibit the growth of CRC cells and induce apoptosis, which may be related to the up-regulation of ESR2 and inhibition of the PI3K/Akt signalling pathway.

Indexed as

colorectal cancerESR2Isoliquiritigeninnetwork pharmacologyPI3K/AKT pathway

Identifiers

PMID38256877
PMCPMC10820227
OpenAlexW4390272628

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.