Evidence map›Paper›PMID 32438972›Full record

ReviewBMB reports2020

Angiogenesis and vasculogenic mimicry as therapeutic targets in ovarian cancer.

Dansaem Lim, Yeojin Do, Byung Su Kwon, Woochul Chang, Myeong-Sok Lee, Jongmin Kim, Jin Gu Cho

Open access · goldAbstract readReview
In one paragraph

Review in BMB reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

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  16. International journal of molecular sciences · 2024
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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

7 authors at 3 institutions in 2 countries.

Dansaem LimDivision of Biological Sciences, Sookmyung Women's University, Seoul 04310, Korea.
Yeojin DoDivision of Biological Sciences, Sookmyung Women's University, Seoul 04310, Korea.
Byung Su KwonDepartment of Obstetrics and Gynecology, Pusan National University School of Medicine, Biomedical Research Institute, Pusan National University Hospital, Busan 49241, Korea.
Woochul ChangDepartment of Biology Education, College of Education, Pusan National University, Busan 46241, Korea.
Myeong-Sok LeeDivision of Biological Sciences, Sookmyung Women's University, Seoul 04310; Research Institute for Women's Health, Sookmyung Women's University, Seoul 04310, Korea.
Jongmin KimDivision of Biological Sciences, Sookmyung Women's University, Seoul 04310; Research Institute for Women's Health, Sookmyung Women's University, Seoul 04310, Korea.
Jin Gu ChoDivision of Biological Sciences, Sookmyung Women's University, Seoul 04310; Research Institute for Women's Health, Sookmyung Women's University, Seoul 04310, Korea.
Sookmyung Women's University · KRPusan National University · KRPusan National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor angiogenesis is an essential process for growth and metastasis of cancer cells as it supplies tumors with oxygen and nutrients. During tumor angiogenesis, many pro-angiogenic factors are secreted by tumor cells to induce their own vascularization via activation of pre-existing host endothelium. However, accumulating evidence suggests that vasculogenic mimicry (VM) is a key alternative mechanism for tumor vascularization when tumors are faced with insufficient supply of oxygen and nutrients. VM is a tumor vascularization mechanism in which tumors create a blood supply system, in contrast to tumor angiogenesis mechanisms that depend on pre-existing host endothelium. VM is closely associated with tumor progression and poor prognosis in many cancers. Therefore, inhibition of VM may be a promising therapeutic strategy and may overcome the limitations of anti-angiogenesis therapy for cancer patients. In this review, we provide an overview of the current anti-angiogenic therapies for ovarian cancer and the current state of knowledge regarding the links between microRNAs and the VM process, with a focus on the mechanism that regulates associated signaling pathways in ovarian cancer. Moreover, we discuss the potential for VM as a therapeutic strategy against ovarian cancer. [BMB Reports 2020; 53(6): 291-298].

Indexed as

Antineoplastic AgentsFemaleHumansMicroRNAsNeovascularization, PathologicOvarian NeoplasmsSignal TransductionAntineoplastic AgentsMicroRNAs

Identifiers

PMID32438972
PMCPMC7330806
OpenAlexW3028472215

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.