Evidence map›Paper›PMID 32848368›Full record

ArticleDrug design, development and therapy2020

Dual Targeting of Cell Growth and Phagocytosis by Erianin for Human Colorectal Cancer.

Yihan Sun, Guofeng Li, Qi Zhou, Danyue Shao, Jingwei Lv, Jianhua Zhou

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. 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

6 authors at 2 institutions in 1 country.

Yihan SunSchool of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun 130117, People's Republic of China.ORCID 0000-0001-8305-030X
Guofeng LiSchool of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun 130117, People's Republic of China.ORCID 0000-0001-5177-0169
Qi ZhouSchool of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun 130117, People's Republic of China.ORCID 0000-0003-1505-9980
Danyue ShaoSecond School of Clinical Medicine, Beijing University of Chinese Medicine, Beijing 100029, People's Republic of China.ORCID 0000-0002-2858-1519
Jingwei LvJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun 130117, People's Republic of China.
Jianhua ZhouSchool of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun 130117, People's Republic of China.ORCID 0000-0001-8609-7111
Changchun University of Chinese Medicine · CNBeijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of erianin on tumor growth and immune response in human colorectal cancer cells (CRC).

methodsThe effect of erianin on tumor growth was determined by CCK8 and colony formation assay. Western blotting was used to evaluate the expression levels of relevant proteins and qRT-PCR was used to evaluate the mRNA level of the relevant gene. The transcriptional activity of β-catenin was determined by dual-luciferase reporter assay. Cellular thermal shift assay was used to quantify drug-target interactions. The cell surface CD47 was assessed by flow cytometry. The enrichment of H3K27 acetyl marks on CD47 promoter was evaluated by chromatin immunoprecipitation assay. Phagocytosis assay was used to determine the phagocytic activity of macrophage. In vivo role of erianin was studied on xenograft models.

resultsWe found that erianin significantly decreased cell survival, colony formation, induced cell cycle arrest, and led to cell apoptosis in SW480 and HCT116 cells. Mechanism analysis demonstrated that erianin inhibited the nuclear translocation and transcriptional activity of β-catenin, which might result from erianin-β-catenin interaction. In addition, the downstream gene expressions, such as c-Myc and cyclin D1, was decreased. More interestingly, erianin decreased the expression of CD47 by regulating H3K27 acetyl marks enrichment on CD47 promoter. Consequently, macrophage-mediated phagocytosis was increased. Our in vivo experiments further confirmed the inhibitory effect of erianin on tumor growth.

conclusionIn summary, erianin could inhibit CRC cells growth and promoted phagocytosis, which suggested erianin as a potential therapeutic strategy for CRC patients.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicApoptosisBibenzylsCell Cycle CheckpointsCell ProliferationCell SurvivalColorectal NeoplasmsDendrobiumDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMiceMice, Inbred NODMice, SCIDMolecular StructureAntineoplastic Agents, PhytogenicBibenzylsErianinPhenolCD47colorectal cancererianinmacrophageβ-catenin

Identifiers

PMID32848368
PMCPMC7429191
OpenAlexW3048900295

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.