Evidence map›Paper›PMID 31545454›Full record

ArticleOncology reports2019

Downregulated IGFBP7 facilitates liver metastasis by modulating epithelial‑mesenchymal transition in colon cancer.

Yuanfei Li, Yanfeng Xi, Guoqiang Zhu, Junmei Jia, He Huang, Yanyan Liu, Yarong Guo, Lixin Liu

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

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  13. Tumor-Derived Exosomes Modulate Primary Site Tumor Metastasis.Frontiers in cell and developmental biology · 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

8 authors at 3 institutions in 1 country.

Yuanfei LiDepartment of Oncology, The First Clinical Hospital, Shanxi Medical University, Tai'yuan, Shanxi 030001, P.R. China.
Yanfeng XiDepartment of Pathology, Shanxi Cancer Hospital, Tai'yuan, Shanxi 030001, P.R. China.
Guoqiang ZhuDepartment of Burn and Plastic, The 985 Hospital of The PLA, Tai'yuan, Shanxi 030001, P.R. China.
Junmei JiaDepartment of Oncology, The First Hospital, Shanxi Medical University, Tai'yuan, Shanxi 030001, P.R. China.
He HuangDepartment of General Surgery, The First Clinical Hospital, Shanxi Medical University, Tai'yuan, Shanxi 030001, P.R. China.
Yanyan LiuDepartment of Oncology, The First Clinical Hospital, Shanxi Medical University, Tai'yuan, Shanxi 030001, P.R. China.
Yarong GuoDepartment of Oncology, The First Clinical Hospital, Shanxi Medical University, Tai'yuan, Shanxi 030001, P.R. China.
Lixin LiuDepartment of Gastroenterology and Hepatology, The First Clinical Hospital, Shanxi Medical University, Tai'yuan, Shanxi 030001, P.R. China.
First Hospital of Shanxi Medical University · CNShanxi Medical University · CNShanxi Provincial Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Distant metastasis is a major cause of cancer‑associated mortality in patients with colon cancer. Insulin‑like growth factor binding protein 7 (IGFBP7) has been identified as a crucial inhibitor of human cancer. However, the role of IGFBP7 in the pathogenesis of metastatic colon cancer has not been investigated. In the present study, the expression of IGFBP7 in 81 pairs of colon cancer tissues and adjacent normal tissues were investigated using immunohistochemistry. Furthermore, 24 pairs of primary colon cancer and matched liver metastasis tissues were analyzed. LοVο cells with IGFBP7‑knockdown and HT‑29 cells with IGFBP7‑overexpression were employed. The expression levels of E‑cadherin, N‑cadherin and Vimentin were quantified and compared. Significant alterations in the expression of IGFBP7 between late stage (III + IV) colon cancer and adjacent normal colonic mucosa were observed. (P=0.031). The association between IGFBP7 and epithelial‑mesenchymal transition (EMT) markers were validated in primary colon cancer and matched liver metastasis tissues. The invasive front of liver metastatic colon tissues revealed reduced IGFBP7 expression. Additionally, knockdown of IGFBP7 in LοVο cells resulted in decreased E‑cadherin, and increased N‑cadherin and Vimentin expression compared with the control group. Overexpression of IGFBP7 in HT‑29 cells induced an upregulation of E‑cadherin; however, the N‑cadherin and Vimentin levels were decreased. In conclusion, the results of the present study suggested that IGFBP7 may prevent colon cancer metastasis by inhibiting EMT, and serves as a potential diagnostic marker and therapeutic target for patients with colon cancer.

Indexed as

Down-RegulationCaco-2 CellsCell Line, TumorCell MovementCell ProliferationColonic NeoplasmsEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHT29 CellsHumansInsulin-Like Growth Factor Binding ProteinsLiver NeoplasmsMaleNeoplasm Staginginsulin-like growth factor binding protein-related protein 1Insulin-Like Growth Factor Binding Proteins

Identifiers

PMID31545454
PMCPMC6775820
OpenAlexW2971499473

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.