Evidence map›Paper›PMID 29048687›Full record

ArticleOncology reports2017

SP1 promotes tumor angiogenesis and invasion by activating VEGF expression in an acquired trastuzumab‑resistant ovarian cancer model.

Feng Su, Jing Geng, Xinying Li, Chuan Qiao, Longlong Luo, Jiannan Feng, Xinjun Dong, Ming Lv

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-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

27 citing papers in PubMed, 45 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

8 authors at 1 institution in 1 country.

Feng SuDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Jing GengDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Xinying LiDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Chuan QiaoDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Longlong LuoDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Jiannan FengDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Xinjun DongDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Ming LvDepartment of Molecular Immunology, Institute of Basic Medical Science, Academy of Military Medical Sciences, Haidian, Beijing 100850, P.R. China.
Academy of Military Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is one of the most common gynecologic cancers and the leading cause of mortality in women worldwide. HER2/neu is overexpressed in various types of cancers and is most commonly associated with decreased survival. Trastuzumab is a humanized anti-HER2 monoclonal antibody for the treatment of HER2-positive breast cancers. However, primary and/or acquired resistance occurs in up to 62% patients during the first year of treatment. Vascular endothelial growth factor (VEGF) is a well‑known angiogenesis factor involved in many physiological and pathological processes. Its significance has been implicated in promoting tumor growth and metastasis via angiogenesis. In the present study, we demonstrated that the upregulation of SP1 enhanced expression of VEGF promoting the angiogenesis and migration of trastuzumab-resistant ovarian cancer cell line SKOV3-T. Our in vitro and in vivo results both gave evidence that the SP1-VEGF axis was responsible for the enhanced malignancy, angiogenesis and migration in the acquired trastuzumab-resistant ovarian cancer cell model.

Indexed as

Drug Resistance, NeoplasmAnimalsCell Line, TumorCell MovementCell ProliferationFemaleHumansMiceNeoplasm InvasivenessNeoplasm TransplantationNeovascularization, PathologicOvarian NeoplasmsSp1 Transcription FactorTrastuzumabUp-RegulationVascular Endothelial Growth Factor ASP1 protein, humanSp1 Transcription FactorTrastuzumabVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID29048687
PMCPMC5780020
OpenAlexW2757961912

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.