Evidence map›Paper›PMID 37867279›Full record

ReviewCurrent topics in medicinal chemistry2024

Phytochemicals Showing Antiangiogenic Effect in Pre-clinical Models and their Potential as an Alternative to Existing Therapeutics.

Anna Senrung, Tanya Tripathi, Nikita Aggarwal, Divya Janjua, Joni Yadav, Apoorva Chaudhary, Arun Chhokar, Udit Joshi, Alok Chandra Bharti

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current topics in medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Anna SenrungDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Tanya TripathiDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Nikita AggarwalDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Divya JanjuaDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Joni YadavDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Apoorva ChaudharyDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Arun ChhokarDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Udit JoshiDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.
Alok Chandra BhartiDepartment of Zoology, Molecular Oncology Laboratory, University of Delhi (North Campus), Delhi, 110007, India.ORCID 0000-0002-5996-2832

Funding

CCRH 17-51/2016-17/CCRH/Tech/Coll./DU-Cervical Cancer.4850Council of Scientific and Industrial Research (CSIR) 09/045(1622)/2018-EMR-I, 09/045(1629)/2019-EMR-I, 09/0045/(11635)/2021-EMR-1, 09/0045(12901)/2022-EMR-1Indian Council of Medical Research (ICMR-ICRC) 5/13/4/ACB/ICRC/2020/NCD-IIIInstitution of Eminence, University of Delhi IoE/2021/12/FRPUniversity Grants Commission (UGC) 764/(CSIR-UGC NET JUNE 2019, 573(CSIR-UGC NET JUNE 2017)
6 · The paper itself

Abstract

Angiogenesis, the formation of new blood vessels from a pre-existing vascular network, is an important hallmark of several pathological conditions, such as tumor growth and metastasis, proliferative retinopathies, including proliferative diabetic retinopathy and retinopathy of prematurity, age-related macular degeneration, rheumatoid arthritis, psoriasis, and endometriosis. Putting a halt to pathology-driven angiogenesis is considered an important therapeutic strategy to slow down or reduce the severity of pathological disorders. Considering the attrition rate of synthetic antiangiogenic compounds from the lab to reaching the market due to severe side effects, several compounds of natural origin are being explored for their antiangiogenic properties. Employing pre-clinical models for the evaluation of novel antiangiogenic compounds is a promising strategy for rapid screening of antiangiogenic compounds. These studies use a spectrum of angiogenic model systems that include HUVEC two-dimensional culture, nude mice, chick chorioallantoic membrane, transgenic zebrafish, and dorsal aorta from rats and chicks, depending upon available resources. The present article emphasizes the antiangiogenic activity of the phytochemicals shown to exhibit antiangiogenic behavior in these well-defined existing angiogenic models and highlights key molecular targets. Different models help to get a quick understanding of the efficacy and therapeutics mechanism of emerging lead molecules. The inherent variability in assays and corresponding different phytochemicals tested in each study prevent their immediate utilization in clinical studies. This review will discuss phytochemicals discovered using suitable preclinical antiangiogenic models, along with a special mention of leads that have entered clinical evaluation.

Indexed as

Angiogenesis InhibitorsPhytochemicalsAnimalsHumansNeovascularization, PathologicAngiogenesis InhibitorsPhytochemicals2D endothelial cell cultureAntiangiogenic phytochemicals.Chick CAMDorsal aortaNude miceTransgenic zebrafish

Identifiers

PMID37867279

What OpenQuestion holds

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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.