Evidence map›Paper›PMID 39309689›Full record

ArticleMedComm2024

SCR-7952, a highly selective MAT2A inhibitor, demonstrates synergistic antitumor activities in combination with the

Zhiyong Yu, Yi Kuang, Liting Xue, Xuan Ma, Tingting Li, Linlin Yuan, Mengying Li, Grace Xue, Zhen Li, Feng Tang and 5 more

Abstract read
In one paragraph

Article in MedComm, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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

15 authors.

Zhiyong YuState Key Laboratory of Neurology and Oncology Drug Development Nanjing China.
Yi KuangDepartment of Preclinical Research Simcere Zaiming Pharmaceutical Co., Ltd. Shanghai China.
Liting XueState Key Laboratory of Neurology and Oncology Drug Development Nanjing China.
Xuan MaDepartment of Thoracic Surgery The Affiliated Xiangshan Hospital of Wenzhou Medical University Wenzhou Zhejiang China.
Tingting LiDepartment of Preclinical Research Simcere Zaiming Pharmaceutical Co., Ltd. Shanghai China.
Linlin YuanState Key Laboratory of Neurology and Oncology Drug Development Nanjing China.
Mengying LiDepartment of Preclinical Research Simcere Zaiming Pharmaceutical Co., Ltd. Shanghai China.
Grace XueWeston High School Weston Massachusetts USA.
Zhen LiDepartment of Preclinical Research Simcere Zaiming Pharmaceutical Co., Ltd. Shanghai China.
Feng TangState Key Laboratory of Neurology and Oncology Drug Development Nanjing China.
Jianxing TangDepartment of Preclinical Research Simcere Zaiming Pharmaceutical Co., Ltd. Shanghai China.
Jinwen ShanDepartment of Preclinical Research Simcere Zaiming Pharmaceutical Co., Ltd. Shanghai China.
Weijie WangDepartment of Thoracic Surgery The Affiliated Xiangshan Hospital of Wenzhou Medical University Wenzhou Zhejiang China.
Renhong TangState Key Laboratory of Neurology and Oncology Drug Development Nanjing China.
Feng ZhouState Key Laboratory of Neurology and Oncology Drug Development Nanjing China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metabolic enzyme methionine adenosyltransferase 2A (MAT2A) was found to elicit synthetic lethality in methylthioadenosine phosphorylase (

Indexed as

drug combinationMAT2A inhibitorMTAP‐deleted cancerPRMT5

Identifiers

PMID39309689
PMCPMC11413503

What OpenQuestion holds

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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.