Evidence map›Paper›PMID 31911852›Full record

ArticleAmerican journal of cancer research2019

FGFBP1, a downstream target of the FBW7/c-Myc axis, promotes cell proliferation and migration in pancreatic cancer.

Zheng Zhang, Mengqi Liu, Qiangsheng Hu, Wenyan Xu, Wensheng Liu, Qiqing Sun, Zeng Ye, Guixiong Fan, Xiaowu Xu, Xianjun Yu and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. The FGF/FGFR/c-Myc axis as a promising therapeutic target in multiple myeloma.Journal of experimental & clinical cancer research : CR · 2024
    Review
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  7. Abrogation of KLF5 sensitizesActa biochimica et biophysica Sinica · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Target c-Myc to treat pancreatic cancer.Cancer biology & therapy · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

12 authors at 1 institution in 1 country.

Zheng ZhangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Mengqi LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Qiangsheng HuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Wenyan XuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Wensheng LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Qiqing SunDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Zeng YeDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Guixiong FanDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Xiaowu XuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Xianjun YuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Shunrong JiDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Yi QinDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center Shanghai, P. R. China.
Fudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The secreted fibroblast growth factor (FGF) binding protein (FGF-BP), which is an extracellular chaperone molecule for FGFs, has been demonstrated to enhance the biological and biochemical activities of FGFs and to be closely related to the growth of several cancers. However, the role of FGFBP1 in pancreatic adenocarcinoma (PDAC) has not been studied extensively. We previously reported that decreased FBW7 could induce pancreatic cancer proliferation and progression. In the present study, we investigated whether FBW7 inhibited cell proliferation and metastasis by decreasing the expression of FGFBP1 in pancreatic cancer. We initially confirmed that pancreatic cancer patients with higher FGFBP1 expression had a worse prognosis. Next, we demonstrated that FGFBP1 silencing inhibited the proliferation and metastasis of PANC-1 and Mia PaCa-2 cells. Mechanistically, FGFBP1 was negatively correlated with FBW7 but positively correlated with c-Myc in PDAC tissue samples, and FBW7 regulated FGFBP1 in a c-Myc-dependent manner. We also found that FBW7 silencing could partly reverse the effect of FGFBP1 silencing on proliferation and metastasis. In summary, FGFBP1 is a prognostic marker for overall survival and is required for pancreatic cancer cell proliferation and metastasis, which is mediated by FBW7 in a c-Myc-dependent manner. Thus, targeting the FBW7/c-Myc/FGFBP1 axis might suppress recurrence and metastasis and provide novel treatment strategies for PDAC.

Indexed as

c-MycFBW7FGFBP1metastasisPancreatic adenocarcinomaproliferation

Identifiers

PMID31911852
PMCPMC6943353
OpenAlexW2998750175

What OpenQuestion holds

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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.