Evidence map›Paper›PMID 34363022›Full record

ArticleOncogene2021

FBP1 regulates proliferation, metastasis, and chemoresistance by participating in C-MYC/STAT3 signaling axis in ovarian cancer.

Haoran Li, Zihao Qi, Yongdong Niu, Yufei Yang, Mengjiao Li, Yangyang Pang, Mingming Liu, Xi Cheng, Midie Xu, Ziliang Wang

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Haoran Li *Cancer Institute and Department of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Zihao Qi *Department of General Surgery, Shanghai First People's Hospital, Shanghai Jiaotong Univeristy School of Medicine, Shanghai, China.
Yongdong Niu *Department of Pharmacology, Shantou University Medical College, Shantou, China.ORCID http://orcid.org/0000-0002-5392-3736
Yufei YangCancer Institute and Department of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Mengjiao LiCancer Institute and Department of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yangyang PangShanghai Xuhui Central Hospital, Zhongshan-Xuhui Hospital, Fudan University, Shanghai, China.
Mingming LiuSchool of Pharmacy, Anhui Medical University, Hefei, China.
Xi ChengCancer Institute and Department of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai, China. cheng_xi1@hotmail.com.ORCID http://orcid.org/0000-0002-4534-5112
Midie XuDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China. xumd27202003@sina.com.ORCID http://orcid.org/0000-0003-1775-6608
Ziliang WangCancer Institute and Department of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai, China. huf_zlwang@126.com.ORCID http://orcid.org/0000-0002-2702-5887
Shanghai Medical College of Fudan University · CNAnhui Medical University · CNFudan University · CNFudan University Shanghai Cancer Center · CNShanghai First People's Hospital · CNShantou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fructose-1,6-bisphosphatase (FBP1) is a rate-limiting enzyme in gluconeogenesis and an important tumor suppressor in human malignancies. Here, we aimed to investigate the expression profile of FBP1 in ovarian cancer, the molecular mechanisms that regulate FBP1 expression and to examine how the FBP1 regulatory axis contributes to tumorigenesis and progression in ovarian cancer. We showed that FBP1 expression was significantly decreased in ovarian cancer tissues compared with normal ovarian tissues, and low-FBP1 expression predicted poor prognosis in patients with ovarian cancer. The enhanced expression of FBP1 in ovarian cancer cell lines suppressed proliferation and 2-D/3-D invasion, reduced aerobic glycolysis, and sensitized cancer cells to cisplatin-induced apoptosis. Moreover, DNA methylation and C-MYC binding at the promoter inhibited FBP1 expression. Furthermore, through physical interactions with signal transducer and activator of transcription 3 (STAT3), FBP1 suppressed nuclear translocation of STAT3 and exerted its non-metabolic enzymatic activity to induce the dysfunction of STAT3. Thus, our study suggests that FBP1 may be a valuable prognostic predictor for ovarian cancer. C-MYC-dependent downregulation of FBP1 acted as a tumor suppressor via modulating STAT3, and the C-MYC/FBP1/STAT3 axis could be a therapeutic target.

Indexed as

AnimalsCell ProliferationDNA-Binding ProteinsFemaleFructose-BisphosphataseHumansMiceMice, NudeNeoplasm MetastasisOvarian NeoplasmsSignal TransductionSTAT3 Transcription FactorTranscription FactorsTransfectionDNA-Binding ProteinsFBP1 protein, humanFructose-BisphosphataseMYCBP protein, humanSTAT3 Transcription FactorTranscription Factors

Identifiers

PMID34363022
PMCPMC8497274
OpenAlexW3191848403

What OpenQuestion holds

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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.