Evidence map›Paper›PMID 36982637›Full record

ReviewInternational journal of molecular sciences2023

Promising Strategy of mPTP Modulation in Cancer Therapy: An Emerging Progress and Future Insight.

Mohammad Waseem, Bi-Dar Wang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. 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
5.8field-weighted citation impact, top 3% 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, 38 citations in OpenAlex.

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  18. Apoptosis and eryptosis: similarities and differences.Apoptosis : an international journal on programmed cell death · 2024
    Review
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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

2 authors at 2 institutions in 1 country.

Mohammad WaseemDepartment of Pharmaceutical Sciences, School of Pharmacy and Health Professions, University of Maryland Eastern Shore, Princess Anne, MD 21853, USA.ORCID 0000-0002-1708-0137
Bi-Dar WangDepartment of Pharmaceutical Sciences, School of Pharmacy and Health Professions, University of Maryland Eastern Shore, Princess Anne, MD 21853, USA.ORCID 0000-0002-2530-7020
University of Maryland, Baltimore · USUniversity of Maryland Eastern Shore · US

Funding

Aberrant Splice Variants as Potential Precision Biomarkers for Aggressive Prostate Cancers in African American PatientsSC1GM127256 · NIGMS · UNIVERSITY OF MARYLAND EASTERN SHORE · PI WANG, BI-DAR · 2019 to 2022
$1.6M
NIGMS NIH HHS 5SC1GM127256NIGMS NIH HHS SC1 GM127256
6 · The paper itself

Abstract

Cancer has been progressively a major global health concern. With this developing global concern, cancer determent is one of the most significant public health challenges of this era. To date, the scientific community undoubtedly highlights mitochondrial dysfunction as a hallmark of cancer cells. Permeabilization of the mitochondrial membranes has been implicated as the most considerable footprint in apoptosis-mediated cancer cell death. Under the condition of mitochondrial calcium overload, exclusively mediated by oxidative stress, an opening of a nonspecific channel with a well-defined diameter in mitochondrial membrane allows free exchange between the mitochondrial matrix and the extra mitochondrial cytosol of solutes and proteins up to 1.5 kDa. Such a channel/nonspecific pore is recognized as the mitochondrial permeability transition pore (mPTP). mPTP has been established for regulating apoptosis-mediated cancer cell death. It has been evident that mPTP is critically linked with the glycolytic enzyme hexokinase II to defend cellular death and reduce cytochrome c release. However, elevated mitochondrial Ca

Indexed as

Mitochondrial Membrane Transport ProteinsNeoplasmsApoptosisCalciumCell DeathMitochondriaMitochondrial Permeability Transition PoreCalciumMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreMOMPmPTPmPTP-mediated apoptosisoxidative stresstherapeutic targets

Identifiers

PMID36982637
PMCPMC10051994
OpenAlexW4324383475

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.