Evidence map›Paper›PMID 32304027›Full record

ArticleHuman cell2020

AGR2-induced glucose metabolism facilitated the progression of endometrial carcinoma via enhancing the MUC1/HIF-1α pathway.

Wei Gong, Belize Ekmu, Xinmei Wang, Yanli Lu, Li Wan

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-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

24 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Role of ENO1 and its targeted therapy in tumors.Journal of translational medicine · 2024
    Review
  8. Article
  9. Review
  10. Review
  11. Potential Role of AGR2 for Mammalian Skin Wound Healing.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. From development to cancer - an ever-increasing role of AGR2.American journal of cancer research · 2021
    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

5 authors at 1 institution in 1 country.

Wei GongDepartment of Gynaecology, The Fourth Affiliated Hospital of Xinjiang Medical University, No. 116 Huanghe Road, Tianshan District, Urumqi City, 830000, Xinjiang Uygur Autonomous Region, China. WeiGongdjk@163.com.
Belize EkmuDepartment of Gynaecology, The Fourth Affiliated Hospital of Xinjiang Medical University, No. 116 Huanghe Road, Tianshan District, Urumqi City, 830000, Xinjiang Uygur Autonomous Region, China.
Xinmei WangDepartment of Gynaecology, The Fourth Affiliated Hospital of Xinjiang Medical University, No. 116 Huanghe Road, Tianshan District, Urumqi City, 830000, Xinjiang Uygur Autonomous Region, China.
Yanli LuDepartment of Gynaecology, The Fourth Affiliated Hospital of Xinjiang Medical University, No. 116 Huanghe Road, Tianshan District, Urumqi City, 830000, Xinjiang Uygur Autonomous Region, China.
Li WanDepartment of Gynaecology, The Fourth Affiliated Hospital of Xinjiang Medical University, No. 116 Huanghe Road, Tianshan District, Urumqi City, 830000, Xinjiang Uygur Autonomous Region, China.
Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anterior gradient 2 (AGR2) was proved to modulate cancer progression. However, the role of AGR2 on endometrial cancer was not established. Here, we investigated the effects of AGR2 expression on endometrial cancer and explored the regulation mechanism. In the study, we found that AGR2 was overexpressed in tumor tissues of 30 endometrial cancer patients. A high level of AGR2 promoted endometrial cancer cells proliferation, migration and invasion. AGR2 induced the expression of lactate dehydrogenase A (LDHA), phosphoglycerate kinase 1 (PGK1), kallikrein 2 (HK2), and enolase 1-α (ENO1), glucose uptake and lactate production. AGR2 could bind to MUC1 and induce MUC1 and hypoxia-inducible factor 1α (HIF-1α). The inhibition effects of AGR2 knockdown on cells proliferation, migration and invasion ability were abolished by the overexpression of MUC1. Besides, the overexpression of MUC1 also reversed the inhibition effects of AGR2 knockdown on the expression of LDHA, HK2, PGK1 and ENO1, glucose uptake and lactate production. AGR2 knockdown inhibited tumor growth, the levels of Ki-67, MUC1, HIF-1α and glycolysis. In conclusion, AGR2 was overexpressed in endometrial cancer and AGR2-induced glucose metabolism facilitated the progression of endometrial carcinoma via the MUC1/HIF-1α pathway. AGR2 may be an effective therapeutic target for endometrial carcinoma.

Indexed as

Biomarkers, TumorCarcinomaCell MovementCell ProliferationDisease ProgressionDNA-Binding ProteinsEndometrial NeoplasmsFemaleGene ExpressionGlucoseHexokinaseHumansHypoxia-Inducible Factor 1, alpha SubunitL-Lactate DehydrogenaseMolecular Targeted TherapyMucin-1AGR2 protein, humanBiomarkers, TumorDNA-Binding ProteinsENO1 protein, humanGlucoseHexokinaseHIF1A protein, humanHK2 protein, humanHypoxia-Inducible Factor 1, alpha SubunitLDHA protein, humanL-Lactate DehydrogenaseMUC1 protein, humanMucin-1MucoproteinsOncogene ProteinsPGK1 protein, humanPhosphoglycerate KinasePhosphopyruvate HydrataseTumor Suppressor ProteinsAGR2Endometrial carcinomaGlucose metabolismHIF-1αMUC1

Identifiers

PMID32304027
OpenAlexW3016666353

What OpenQuestion holds

Textmetadata
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.