Evidence map›Paper›PMID 36550099›Full record

ArticleCell death & disease2022

ABX-1431 inhibits the development of endometrial adenocarcinoma and reverses progesterone resistance by targeting MGLL.

Xiaohong Ma, Min Xia, Lina Wei, Kui Guo, Rui Sun, Yao Liu, Chunping Qiu, Jie Jiang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. The biological functions of monoacylglycerol lipase (MAGL) in cancer.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
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  8. mTORC1 regulates the proliferation of SOX9Histochemistry and cell biology · 2025
    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

8 authors at 2 institutions in 1 country.

Xiaohong Ma *Department of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China.ORCID 0000-0001-8625-237X
Min Xia *Department of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China.
Lina WeiDepartment of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China.
Kui GuoDepartment of Gynecology and Obstetrics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, 264000, Yantai, China.ORCID 0000-0002-3594-3901
Rui SunDepartment of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China.
Yao LiuDepartment of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China.
Chunping QiuDepartment of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China. qlyyqcp1124@126.com.ORCID 0000-0003-4625-8165
Jie JiangDepartment of Gynecology and Obstetrics, Qilu Hospital of Shandong University, 250012, Jinan, China. qljiangjie@sdu.edu.cn.ORCID 0000-0002-9634-4152
Qilu Hospital of Shandong University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial cancer is a common gynecological malignancy. With the onset of EC patients younger, conservative treatment with progesterone has become an important option for patients trying to preserve reproductive function. However, progesterone resistance is a key factor affecting the efficacy of therapy and it is urgent to clarify the mechanism so as to propose a potential target and inhibit the development of endometrial adenocarcinoma and progesterone resistance. MGLL, an important factor involved in lipid mobilization, is overexpressed in many tumors, however the biological function of MGLL in the development of endometrial adenocarcinoma and the process of progesterone resistance still remains unclear. In this study, we first found MGLL was highly expressed in progesterone resistant samples of endometrial adenocarcinoma, and then we verified its expression was increased in endometrial adenocarcinoma. Through in vitro and in vivo experiments, we demonstrated that overexpression of MGLL promoted tumor proliferation, metastasis and the occurrence of progestogen resistance, knockdown MGLL inhibited tumor proliferation, metastasis and reversed progestogen resistance. In addition, knockdown of MGLL can sensitize endometrial adenocarcinoma cells to progesterone, possibly by affecting ROS generation and reducing the expression of AKR1C1. Finally, it was verified that ABX-1431, MGLL inhibitor, reversed progesterone resistance and enhanced the sensitivity of endometrial adenocarcinoma to progesterone both in vitro and in vivo. In conclusion, the high expression of MGLL is involved in the occurrence and development of endometrial adenocarcinoma and progesterone resistance. Targeted inhibition of MGLL by inhibitors may be an effective method for the treatment of progesterone resistance in endometrial adenocarcinoma.

Indexed as

AdenocarcinomaEndometrial NeoplasmsUterine NeoplasmsEndometriumFemaleHumansPiperazinesProgesteroneProgestinsPyrrolidinesReceptors, ProgesteroneUterine DiseasesABX-1431PiperazinesProgesteroneProgestinsPyrrolidinesReceptors, Progesterone

Identifiers

PMID36550099
PMCPMC9780207
OpenAlexW4312155102

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.