Allyl isothiocyanate regulates oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion and metastasis via interaction with multiple cell signaling pathways
Cancer growth is a molecular mechanism initiated by genetic and epigenetic modifications that are involved in cell proliferation, differentiation, apoptosis, and senescence pathways. Chemoprevention is an important strategy for cancer treatment that leads to blocking, reversing, or impeding the mult...
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description | Cancer growth is a molecular mechanism initiated by genetic and epigenetic modifications that are involved in cell proliferation, differentiation, apoptosis, and senescence pathways. Chemoprevention is an important strategy for cancer treatment that leads to blocking, reversing, or impeding the multistep process of tumorigenesis, including the blockage of its vital morphogenetic milestones viz. normal, preneoplasia, neoplasia, and metastasis. Naturally occurring phytochemicals are becoming ever more popular compared to synthetic drugs for many reasons, including safety, bioavailability, efficacy, and easy availability. Allyl isothiocyanate (AITC) is a natural compound present in all plants of the Cruciferae family, such as Brussels sprouts, cauliflower, mustard, cabbage, kale, horseradish, and wasabi. In vitro and in vivo studies carried out over the decades have revealed that AITC inhibits tumorigenesis without any toxicity and undesirable side effects. The bioavailability of AITC is exceedingly high, as it was reported that nearly 90% of orally administered AITC is absorbed. AITC exhibits multiple pharmacological properties among which its anticancer activity is the most significant for cancer treatment. Its anticancer activity is exerted via selective modulation of multiple cell signaling pathways related to oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion, and metastasis. This review highlights the current knowledge on molecular targets that are involved in the anticancer effect of AITC associated with (i) inhibition of carcinogenic activation and induction of antioxidants, (ii) suppression of pro-inflammatory and cell proliferative signals, (iii) induction of cell cycle arrest and apoptosis, and (iv) inhibition of angiogenic and invasive signals related to metastasis. |
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AITC exhibits multiple pharmacological properties among which its anticancer activity is the most significant for cancer treatment. Its anticancer activity is exerted via selective modulation of multiple cell signaling pathways related to oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion, and metastasis. 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AITC exhibits multiple pharmacological properties among which its anticancer activity is the most significant for cancer treatment. Its anticancer activity is exerted via selective modulation of multiple cell signaling pathways related to oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion, and metastasis. This review highlights the current knowledge on molecular targets that are involved in the anticancer effect of AITC associated with (i) inhibition of carcinogenic activation and induction of antioxidants, (ii) suppression of pro-inflammatory and cell proliferative signals, (iii) induction of cell cycle arrest and apoptosis, and (iv) inhibition of angiogenic and invasive signals related to metastasis.</description><subject>Allyl isothiocyanate</subject><subject>Angiogenesis</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Bioavailability</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer therapies</subject><subject>Carcinogenesis</subject><subject>Cell Biology</subject><subject>Cell cycle</subject><subject>Cell Cycle Checkpoints</subject><subject>Cell differentiation</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Cell signaling</subject><subject>Developmental Biology</subject><subject>Epigenetics</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammation - drug therapy</subject><subject>Isothiocyanates</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Molecular modelling</subject><subject>Oral administration</subject><subject>Oxidative Stress</subject><subject>Preneoplasia</subject><subject>Review</subject><subject>Senescence</subject><subject>Signal Transduction</subject><subject>Toxicity</subject><subject>Tumorigenesis</subject><issn>0948-6143</issn><issn>1432-119X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcmO1DAUtBCIaQZ-gAOyxIVDB7wknfg4GrFJI3EBiVvkLWmPHDvYTg_5Rz6K193DIg5ItmzXq6rnp0LoOSWvKSHtm0xITbuKMA6bNU0lHqANrTmrKBVfH6INEXVX7QC5QE9yviWENoKxx-iCd4QKJugG_bjyfvXY5Vj2LupVBlksTnZcPFwyjt-dkcUdLM4l2Zy32IXBy2kCMIYt1tZ7PKfo3WDT35hetbdYJhCVLZZznEvMDvQyjC6ONtjTy4WDzKAC2ODJFplhuYwPTkKtgKc-muI7V_Z4WnxxM9ieOmQ3BuldGPEsy_5OrvkpejRIn-2z-_MSfXn39vP1h-rm0_uP11c3leZtU6qhNm1NOmM0MQ1jQlHLWkuU4nZn2U52jdRSda3hDRHKNFKpTquhVdwMjNYtv0Svzr4w-LcFBuwnl49_ksHGJfesEw3bMd5SoL78h3oblwT_BpYAgqhZy4DFziydYs7JDv2c3CTT2lPSH7Puz1n3kHV_yroXIHpxb72oyZrfkl_hAoGfCRlKYbTpT-__2P4ENf27qg</recordid><startdate>20240301</startdate><enddate>20240301</enddate><creator>Rajakumar, Thangarasu</creator><creator>Pugalendhi, Pachaiappan</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0811-1533</orcidid><orcidid>https://orcid.org/0000-0003-1168-8464</orcidid></search><sort><creationdate>20240301</creationdate><title>Allyl isothiocyanate regulates oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion and metastasis via interaction with multiple cell signaling pathways</title><author>Rajakumar, Thangarasu ; 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AITC exhibits multiple pharmacological properties among which its anticancer activity is the most significant for cancer treatment. Its anticancer activity is exerted via selective modulation of multiple cell signaling pathways related to oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion, and metastasis. 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subjects | Allyl isothiocyanate Angiogenesis Antitumor activity Apoptosis Bioavailability Biochemistry Biomedical and Life Sciences Biomedicine Cancer therapies Carcinogenesis Cell Biology Cell cycle Cell Cycle Checkpoints Cell differentiation Cell growth Cell Line, Tumor Cell Proliferation Cell signaling Developmental Biology Epigenetics Humans Inflammation Inflammation - drug therapy Isothiocyanates Metastases Metastasis Molecular modelling Oral administration Oxidative Stress Preneoplasia Review Senescence Signal Transduction Toxicity Tumorigenesis |
title | Allyl isothiocyanate regulates oxidative stress, inflammation, cell proliferation, cell cycle arrest, apoptosis, angiogenesis, invasion and metastasis via interaction with multiple cell signaling pathways |
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