Evidence map›Paper›PMID 41781859›Full record

ReviewMolecular medicine (Cambridge, Mass.)2026

Topoisomerase inhibitors in cervical cancer: mechanistic insights and therapeutic strategies.

Yashaswini Reddy, Padmini Pai, Ipshita Das, Shruthi Nayak, Neil Viren D'Souza, Manasa Gangadhar Shetty, Babitha Kampa Sundara

Abstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 2026. 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

7 authors.

Yashaswini ReddyDepartment of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Padmini PaiDepartment of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Ipshita DasDepartment of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Shruthi NayakManipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Neil Viren D'SouzaDepartment of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Manasa Gangadhar ShettyDepartment of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Babitha Kampa SundaraDepartment of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India. babitha.ks@manipal.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer represents a critical global health burden, particularly among women in countries with limited healthcare infrastructure, where it accounts for a substantial proportion of cancer-related morbidity and mortality. It remains highly prevalent in developing regions. Most cervical cancers are squamous cell carcinomas originating from the cervix lining cells, mainly because of chronic infection with high-risk human papillomaviruses (HPV) types. Additionally, the likelihood of infection is enhanced by behaviours include early sexual activity, multiple partners, smoking, and immunosuppression. Topoisomerases, vital enzymes for DNA replication and transcription are crucial for therapeutic intervention in cancer. Inhibitors of Topoisomerase I and II, such as camptothecin derivatives (topotecan, irinotecan) and drugs like etoposide and daunorubicin, have shown effectiveness in treating cancers, including cervical cancer, by stabilizing topoisomerase-DNA complexes and inducing lethal DNA strand breaks. However, traditional treatments like chemotherapy and radiation often have high toxicity and limited survival benefits. The development of new topoisomerase inhibitors with better efficacy and safety is essential. Advances in tumour biology have led to multi targeting drugs that target multiple cancer cells survival pathways, offering a more comprehensive anti-cancer effect. This review explores the application of topoisomerase inhibitors in advanced and recurrent stages of cervical cancer, both as standalone agents and in combination therapies. Combining topoisomerase inhibitors with other treatment options has been used as a strategy to improve therapeutic outcomes. Additionally new therapeutic strategies like nanoformulations, antibody drug conjugates, and biomarker-based therapies lead to effective therapeutic outcomes in cervical cancer treatment. Ongoing research and development in this area are crucial for enhancing cervical cancer treatment.

Indexed as

Antineoplastic AgentsTopoisomerase InhibitorsUterine Cervical NeoplasmsAnimalsFemaleHumansMolecular Targeted TherapyAntineoplastic AgentsTopoisomerase InhibitorsCervical cancerDosageInhibitorsTopoisomerase I and IIToxicityTreatment efficacy

Identifiers

PMID41781859
PMCPMC13069826

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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.