Evidence map›Paper›PMID 35743145›Full record

ReviewInternational journal of molecular sciences2022

ROS and miRNA Dysregulation in Ovarian Cancer Development, Angiogenesis and Therapeutic Resistance.

David C Stieg, Yifang Wang, Ling-Zhi Liu, Bing-Hua Jiang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 50 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

4 authors at 1 institution in 1 country.

David C StiegDepartment of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.ORCID 0000-0003-2746-3315
Yifang WangDepartment of Pathology, Anatomy & Cell Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Ling-Zhi LiuDepartment of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.ORCID 0000-0001-9234-457X
Bing-Hua JiangDepartment of Pathology, Anatomy & Cell Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.ORCID 0000-0003-4526-2031
Thomas Jefferson University · US

Funding

Mechanism of lung cancer resistance to tyrosine kinase inhibitor and radiation treatmentsR01CA232587 · NCI · UNIVERSITY OF IOWA · PI SIMONE, NICOLE L · 2018 to 2022
$2.9M
MiR-152/PKM2/SLC7A5 axis in breast cancer development, chemo- and radiation-treatment responseR01CA263506 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Jun He · 2022 to 2026
$2.8M
METTL3 in chromium-induced angiogenesis and carcinogenesisR01ES033197 · NIEHS · THOMAS JEFFERSON UNIVERSITY · PI STEVEN B. MCMAHON · 2022 to 2026
$2.6M
New Mechanism of Arsenic CarcinogenesisK02ES029119 · NIEHS · UNIVERSITY OF IOWA · PI LIU, LING-ZHI · 2018 to 2022
$613k
American Cancer Society NEC-129306NCI NIH HHS R01CA232587NCI NIH HHS R01CA263506NIEHS NIH HHS K02ES029119NIEHS NIH HHS R01ES024151NIEHS NIH HHS R01ES033197Pennsylvania Department of Health SAP#41000
6 · The paper itself

Abstract

The diverse repertoires of cellular mechanisms that progress certain cancer types are being uncovered by recent research and leading to more effective treatment options. Ovarian cancer (OC) is among the most difficult cancers to treat. OC has limited treatment options, especially for patients diagnosed with late-stage OC. The dysregulation of miRNAs in OC plays a significant role in tumorigenesis through the alteration of a multitude of molecular processes. The development of OC can also be due to the utilization of endogenously derived reactive oxygen species (ROS) by activating signaling pathways such as PI3K/AKT and MAPK. Both miRNAs and ROS are involved in regulating OC angiogenesis through mediating multiple angiogenic factors such as hypoxia-induced factor (HIF-1) and vascular endothelial growth factor (VEGF). The NAPDH oxidase subunit NOX4 plays an important role in inducing endogenous ROS production in OC. This review will discuss several important miRNAs, NOX4, and ROS, which contribute to therapeutic resistance in OC, highlighting the effective therapeutic potential of OC through these mechanisms.

Indexed as

MicroRNAsOvarian NeoplasmsCarcinoma, Ovarian EpithelialDrug Resistance, NeoplasmFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitNADPH OxidasesNeovascularization, PathologicPhosphatidylinositol 3-KinasesReactive Oxygen SpeciesVascular Endothelial Growth Factor AHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsNADPH OxidasesPhosphatidylinositol 3-KinasesReactive Oxygen SpeciesVascular Endothelial Growth Factor AangiogenesisHER3HIF1-αmiRNA dysregulationNOX4ovarian cancerROStherapeutic resistanceVEGF

Identifiers

PMID35743145
PMCPMC9223852
OpenAlexW4283017392

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.