Evidence map›Paper›PMID 37429893›Full record

ArticleScientific reports2023

Liquid tumor microenvironment enhances WNT signaling pathway of peritoneal metastasis of gastric cancer.

Huawei Xu, Zhibin Hao, Yujie Wang, Deng Zhang, Jie Li, Ling Chen, Ninghua Yao, Binbin Qian, Xiaobo Peng, Xianbao Zhan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
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

10 authors at 4 institutions in 1 country.

Huawei Xu *Department of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China.
Zhibin Hao *Department of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China.
Yujie Wang *Department of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China.
Deng ZhangResearch and Early Development, Haobai Biotechnology Inc, Shanghai, 200235, China.
Jie LiDepartment of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China.
Ling ChenDepartment of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China.
Ninghua YaoDepartment of Oncology, Affiliated Hospital of Nantong University, Nantong, 226000, China.
Binbin QianDepartment of Oncology, Tongzhou People's Hospital, Nantong, 226300, China.
Xiaobo PengDepartment of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China. pxb023@126.com.
Xianbao ZhanDepartment of Oncology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China. zhan.xianbao@smmu.edu.cn.
Second Military Medical University · CNChanghai Hospital · CNAffiliated Hospital of Nantong University · CNShanghai CASB Biotechnology (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer remains one of the most prevalent tumors worldwide and peritoneal metastasis is responsible for approximately 60% of death in advanced gastric cancer patients. However, the underlying mechanism of peritoneal metastasis is poorly understood. We have established organoids derived from malignant ascites (MA) of gastric cancer patients and noticed that MA supernatant could strongly increase the colony formation of organoids. Thus, we realized the interaction between exfoliated cancer cells (ECCs) and liquid tumor microenvironment contributes to peritoneal metastasis. Further, we designed a medium component control test which proved that exosomes derived from MA could not enhance the growth of organoids. Using Immunofluorescence and confocal imaging as well as dual-luciferase reporter assay, our data showed WNT signaling pathway was upregulated by high concentrations of WNT ligands (wnt3a and wnt5a), which was verified by ELISA. Besides, suppressing WNT signaling pathway diminished the growth promoting function of MA supernatant. This result implicated WNT signaling pathway as a potential therapeutic target for peritoneal metastasis of gastric cancer.

Indexed as

Peritoneal NeoplasmsStomach NeoplasmsHumansPeritoneumTumor MicroenvironmentWnt Signaling Pathway

Identifiers

PMID37429893
PMCPMC10333202
OpenAlexW4383737843

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.