Evidence map›Paper›PMID 31041640›Full record

ArticleDigestive diseases and sciences2019

Fructose-Bisphosphate Aldolase A Regulates Hypoxic Adaptation in Hepatocellular Carcinoma and Involved with Tumor Malignancy.

Xin Li, Fengxing Jiang, Zhong Ge, Bin Chen, Jiang Yu, Mingjun Xin, Jiandong Wang, Lingxuan An, Jichao Wei, Liqun Wu

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In one paragraph

Article in Digestive diseases and sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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  13. Targeting Energy Metabolism in Cancer Treatment.International journal of molecular sciences · 2022
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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 3 institutions in 1 country.

Xin LiDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Fengxing JiangDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Zhong GeDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Bin ChenDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Jiang YuDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Mingjun XinDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Jiandong WangDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Lingxuan AnDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Jichao WeiDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao University, No.1 Jiaozhou Road, Shibei District, Qingdao City, 266011, Shandong Province, China.
Liqun WuDepartment of Hepatobiliary and Pancreatic Surgery Center of Medical Research, Affiliated Hospital of Qingdao University, No.16 Jiangsu Road, Shinan District, Qingdao City, 266003, Shandong Province, China. wulqqd@163.com.
Qingdao University · CNQingdao Municipal Hospital · CNAffiliated Hospital of Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypoxia is an important factor in malignant tumors, and glycolysis is a major metabolic contributor in their development. Glycolytic enzymes have gained increasing attention as potential therapeutic targets because they are associated with cancer-specific metabolism. Fructose-bisphosphate aldolase A (ALDOA), a key glycolytic enzyme, reportedly is associated with hepatocellular carcinoma (HCC). However, its role in pathogenesis and its clinical significance in HCC remain largely unknown.

aimTo explore the increased expression of ALDOA in HCC in correlation with tumor malignancy, and to investigate the potential regulatory role ALDOA plays in HCC progression through its regulation in hypoxia adaptation. METHODS AND

resultsTo better understand ALDOA and its correlation with clinicopathological features of HCC, we analyzed 100 HCC clinical specimens using immunohistochemistry analysis. The results show that the ALDOA expression level is significantly higher in advanced HCC and in HCC with venous invasion. Using in vitro knockdown assays, we showed that higher ALDOA expression was positively associated with cell proliferation, cell cycle, apoptosis, and invasion under both normoxic and hypoxic conditions. Evidence shows that the underlying mechanism is due to the regulatory function of ALDOA in glycolysis, the cell cycle, matrix metalloproteinase-mediated extracellular matrix degradation, and epithelial-mesenchymal transformation.

conclusionsData indicated that ALDOA is significantly upregulated in HCC tissue and is closely related to HCC malignancy. ALDOA is likely to regulate HCC progression by regulating HCC tumor cell proliferation, apoptosis, and invasion in both normoxic and hypoxic condition.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularCell ProliferationFructose-Bisphosphate AldolaseHep G2 CellsHumansLiver NeoplasmsNeoplasm InvasivenessTumor HypoxiaALDOA protein, humanBiomarkers, TumorFructose-Bisphosphate AldolaseEpithelial–mesenchymal transitionFructose-bisphosphate aldolase AHepatocellular carcinomaHypoxiaMatrix metalloproteinase

Identifiers

PMID31041640
OpenAlexW2943317855

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.