Evidence map›Paper›PMID 38288813›Full record

ReviewCurrent medicinal chemistry2024

Targeting Cervical Cancer Stem Cells by Phytochemicals.

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

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Phytochemicals as Therapeutic Agents against Cancer.Current medicinal chemistry · 2024
    Article
  5. Article
  6. Review
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.

Tanya TripathiMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Joni YadavMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Divya JanjuaMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Apoorva ChaudharyMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Udit JoshiMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Anna SenrungMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Arun ChhokarMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Nikita AggarwalMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.
Alok Chandra BhartiMolecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CaCx) poses a significant global health challenge, ranking as the fourth most common cancer among women worldwide. Despite the emergence of advanced treatment strategies, recurrence remains a bottleneck in favorable treatment outcomes and contributes to poor prognosis. The chemo- or radio-therapy resistance coupled with frequent relapse of more aggressive tumors are some key components that contribute to CaCx-related mortality. The onset of therapy resistance and relapse are attributed to a small subset of, slow-proliferating Cancer Stem Cells (CSC). These CSCs possess the properties of tumorigenesis, self-renewal, and multi-lineage differentiation potential. Because of slow cycling, these cells maintain themselves in a semi-quiescent stage and protect themselves from different anti-proliferative anti-cancer drugs. Keeping in view recent advances in their phenotypic and functional characterization, the feasibility of targeting CSC and associated stem cell signaling bears a strong translational value. The presence of CSC has been reported in CaCx (CCSC) which remains a forefront area of research. However, we have yet to identify clinically useful leads that can target CCSC. There is compelling evidence that phytochemicals, because of their advantages over synthetic anticancer drugs, could emerge as potential therapeutic leads to target these CCSCs. The present article examined the potential of phytochemicals with reported anti-CSC properties and evaluated their future in preclinical and clinical applications against CaCx.

Indexed as

Neoplastic Stem CellsPhytochemicalsUterine Cervical NeoplasmsAnimalsAntineoplastic Agents, PhytogenicFemaleHumansAntineoplastic Agents, PhytogenicPhytochemicalsCancer stem cell signalingcervical cancercervical cancer stem cellschemo-resistancephytochemicalsradio-resistance.

Identifiers

PMID38288813

What OpenQuestion holds

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Registered trials

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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.