Evidence map›Paper›PMID 33683556›Full record

ArticleMolecular and cellular biochemistry2021

Tectoridin inhibits the progression of colon cancer through downregulating PKC/p38 MAPK pathway.

Lingfan Xiong, Wenhao Guo, Yong Yang, Danping Gao, Jun Wang, Yuanyuan Qu, Ying Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

7 authors at 1 institution in 1 country.

Lingfan Xiong *Department of Oncology, China Resources & WISCO General Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, 430080, Hubei, China.
Wenhao GuoDepartment of Oncology, China Resources & WISCO General Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, 430080, Hubei, China. 573514@qq.com.ORCID http://orcid.org/0000-0003-0562-339X
Yong Yang *Department of Oncology, The Second Hospital of WlSCO, Wuhan, 430085, Hubei, China.
Danping GaoDepartment of Obstetrics and Gynaecology, Wuhan Hongshan District Maternal and Child Health Care Hospital, Wuhan, 430073, Hubei, China.
Jun WangDepartment of Oncology, China Resources & WISCO General Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, 430080, Hubei, China.
Yuanyuan QuDepartment of Oncology, The Second Hospital of WlSCO, Wuhan, 430085, Hubei, China.
Ying ZhangDepartment of Oncology, China Resources & WISCO General Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, 430080, Hubei, China.
China Resources (China) · CN

Funding

Hubei Province health and family planning scientific research Project 2018 No. WJ2018H0097
6 · The paper itself

Abstract

Colon cancer is one of the most familiar malignancies worldwide, with high morbidity and high mortality. This study intended to explore the role and mechanism of tectoridin (TEC) in regulating the progression of colon cancer. First, colon cancer cell lines (HCT116 and SW480 cells) were treated with different doses of TEC (0-200 μM). Then, CCK8 and clone formation experiments were performed to detect cell proliferation. Flow cytometry and western blot were conducted to examine apoptosis. Subsequently, Transwell assay and wound-healing test was employed to determine the effect of TEC on colon cancer cell invasion and migration. Next, western blot was performed to monitor the PKC/p38 MAPK pathway activation. In addition, a tumor model was established in nude mice to explore the effect of TEC on tumor growth in vivo. TEC dose-dependently dampened the proliferation, migration and invasion of colon cancer cells and facilitated their apoptosis. In addition, TEC abated the tumor cell growth in vivo. Besides, TEC dose-dependently suppressed the expression of PKC and p38 MAPK. Moreover, inhibiting the PKC pathway almost cancel out the anti-tumor effects induced by TEC. TEC attenuates the colon cancer progression by inhibiting the PKC/p38 MAPK pathway.

Indexed as

Colonic NeoplasmsDown-RegulationGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHCT116 CellsHumansIsoflavonesMAP Kinase Signaling SystemNeoplasm Proteinsp38 Mitogen-Activated Protein KinasesProtein Kinase CIsoflavonesNeoplasm Proteinsp38 Mitogen-Activated Protein KinasesProtein Kinase CtectoridinApoptosisColon cancerPKC/p38 MAPKProliferationTectoridin

Identifiers

PMID33683556
OpenAlexW3133635899

What Socratic 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 Socratic graph.