Evidence map›Paper›PMID 39886791›Full record

ReviewCurrent cancer drug targets2026

Recent Advancements in Drug Targeting for Ferroptosis as an Antitumor Therapy: Development of Novel therapeutics.

Reena Negi Rawat, Sanju Singh, Neeta Gupta, Manish Upadhyay, Shilpi Shrivastava, Bhawana Jain

Abstract readReview
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In one paragraph

Review in Current cancer drug targets, 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

6 authors.

Reena Negi RawatDepartment of Chemistry, Siddhachalam Laboratory, Raipur, 493221, Chhattisgarh, India.
Sanju SinghDepartment of Chemistry, Siddhachalam Laboratory, Raipur, 493221, Chhattisgarh, India.
Neeta GuptaDepartment of Chemistry, Govt. E. Raghavendra Rao P.G. Science College, Bilaspur, Chhattisgarh, 495001, India.
Manish UpadhyayDepartment of Chemistry, ICFAI University, Durg, 490042, Chhattisgarh, India.
Shilpi ShrivastavaDepartment of Chemistry, Kalinga University, Raipur, 492101, Chhattisgarh, India.
Bhawana JainDepartment of Chemistry, Siddhachalam Laboratory, Raipur, 493221, Chhattisgarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe primary objective of this review is to provide updated mechanisms that regulate ferroptosis sensitivity in cancer cells and recent advancements in drug targeting for ferroptosis as an antitumor therapy.

methodsTo achieve these objectives, a comprehensive literature review was conducted, analyzing recent studies on ferroptosis, including its cellular, molecular, and gene-level characteristics. The review involved an evaluation of advancements in ferroptosis drug research across various medical domains, with particular attention to novel therapeutic approaches in nanomedicine, TCM, and Western medicine. The review also included an assessment of how ferroptosis influences cancer treatment, including its role in tumor drug resistance and immunotherapy, and provided a detailed analysis of pharmacological activators of ferroptosis.

resultsThe review highlights several key findings, like primary mechanisms that regulate cancer cell sensitivity to ferroptosis, and provides an overview of the latest advancements in ferroptosis drug research. The review reveals that ferroptosis has both beneficial and detrimental effects on human cancer, reflecting its complex role in cancer progression and treatment. The review also emphasizes the dual nature of ferroptosis, noting its potential as both a tumor suppressor and an oncogenic factor. Additionally, it provides a comprehensive examination of various pharmacological agents that activate ferroptosis and their potential therapeutic applications.

conclusionIn conclusion, ferroptosis represents a promising target for cancer therapy, given its distinctive characteristics and significant role in tumor biology. The review underscores the need for further research to clarify the complex roles of ferroptosis in carcinogenesis and to optimize the development of novel therapeutics targeting this form of cell death. It also highlights current challenges and opportunities in the field, including the potential for overcoming cancer metastasis through ferroptosis modulation and the need for continued exploration of pharmacological activators to advance therapeutic strategies.

Indexed as

Antineoplastic AgentsFerroptosisMolecular Targeted TherapyNeoplasmsAnimalsDrug Resistance, NeoplasmHumansAntineoplastic Agentscancerchemotherapydrug resistanceFerroptosismetastasistargeted therapy.

Identifiers

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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.