Evidence map›Paper›PMID 33221769›Full record

ArticleAging2020

Could microtubule inhibitors be the best choice of therapy in gastric cancer with high immune activity: mutant DYNC1H1 as a biomarker.

Jin Bai, BoWen Yang, Ruichuan Shi, Xinye Shao, Yujing Yang, Fang Wang, Jiawen Xiao, Xiujuan Qu, Yunpeng Liu, Ye Zhang and 1 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Potent therapeutic strategy in gastric cancer with microsatellite instability-high and/or deficient mismatch repair.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
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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 4 institutions in 1 country.

Jin BaiDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
BoWen YangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Ruichuan ShiDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Xinye ShaoDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Yujing YangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Fang WangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Jiawen XiaoDepartment of Medical Oncology, Shenyang Fifth People Hospital, Tiexi District, Shenyang 110001, China.
Xiujuan QuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Yunpeng LiuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Ye ZhangLaboratory I of Cancer Institute, The First Hospital of China Medical University, Shenyang 110001, China.
Zhi LiDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
First Hospital of China Medical University · CNChina Medical University · CNMinistry of Education of the People's Republic of China · CNShenyang Fifth People Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint blockade (ICB) has achieved unprecedented breakthroughs in various cancers, including gastric cancer (GC) with high immune activity (MSI-H or TMB-H), yet clinical benefits from ICB were moderate. Here we aimed to identify the most appropriate drugs which can improve outcomes in GC. We firstly compared MSI-H and TMB-H GC samples with normal samples in TCGA-STAD cohort, respectively. After that, Connectivity Map database repurposed nine candidate drugs (CMap score < -90). Then, microtubule inhibitors (MTIs) were screened as the significant candidate drugs with their representative gene sets strongly enriched (

Indexed as

Tubulin ModulatorsAdenocarcinomaBiomarkers, TumorComputational BiologyCytoplasmic DyneinsDrug DiscoveryHumansMutationStomach NeoplasmsTranscriptomeBiomarkers, TumorCytoplasmic DyneinsDYNC1H1 protein, humanTubulin ModulatorsDYNC1H1gastric cancerimmune checkpoint blockademicrotubule inhibitorsmutation

Identifiers

PMID33221769
PMCPMC7803585
OpenAlexW3107345352

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.