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Cited by 269

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Bacteriocins as Potential Anticancer Agents

Open access
Kaur, Sumanpreet, Kaur, Sukhraj·2015·Frontiers in Pharmacology

Abstract

Cancer remains one of the leading causes of deaths worldwide, despite advances in its treatment and detection. The conventional chemotherapeutic agents used for the treatment of cancer have non-specific toxicity toward normal body cells that cause various side effects. Secondly, cancer cells are known to develop chemotherapy resistance in due course of treatment. Thus, the demand for novel anti-cancer agents is increasing day by day. Some of the experimental studies have reported the therapeutic potential of bacteriocins against various types of cancer cell lines. Bacteriocins are ribosomally-synthesized cationic peptides secreted by almost all groups of bacteria. Some bacteriocins have shown selective cytotoxicity toward cancer cells as compared to normal cells. This makes them promising candidates for further investigation and clinical trials. In this review article, we present the overview of the various cancer cell-specific cytotoxic bacteriocins, their mode of action and efficacies.

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Metadata

Authors
Kaur, S., & Kaur, S.
Venue
Frontiers in Pharmacology
Published
2015-11-10
Volume
6
Pages
272-272
ISSN
1663-9812 (ISSN-L)
OpenAlex
W2176673138
Cited by
269
References
2
FWCI
5.14
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Bacteriocins as Potential Anticancer Agents. https://app.cochat.ai/papers/10.3389/fphar.2015.00272
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Kaur, S., & Kaur, S. (2015). Bacteriocins as Potential Anticancer Agents. Frontiers in Pharmacology. https://doi.org/10.3389/fphar.2015.00272

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.