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Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract

BACKGROUND AND AIM: Although, the anticancer potential of Aqueous Azadirachta indica leaf extract (AAILE) has been robustly established against cutaneous squamous cell carcinoma (SCC) in mice, however, its ability in modulating tumor associated extra cellular matrix (ECM) is largely unknown. Therefo...

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Autores principales: Chugh, N.A., Koul, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116721/
https://www.ncbi.nlm.nih.gov/pubmed/34012866
http://dx.doi.org/10.1016/j.jtcme.2020.03.006
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author Chugh, N.A.
Koul, A.
author_facet Chugh, N.A.
Koul, A.
author_sort Chugh, N.A.
collection PubMed
description BACKGROUND AND AIM: Although, the anticancer potential of Aqueous Azadirachta indica leaf extract (AAILE) has been robustly established against cutaneous squamous cell carcinoma (SCC) in mice, however, its ability in modulating tumor associated extra cellular matrix (ECM) is largely unknown. Therefore, the present study was conceived to explore changes in ECM during murine skin cancer and its chemoprevention by AAILE. EXPERIMENTAL PROCEDURE: Skin tumors were induced using a two-stage model of carcinogenesis employing topical application of 7,12-Dimethylbenz(a)anthracene (DMBA) and 12-O-tetradecanoyl phorbol-13-acetate (TPA) as carcinogen and promoter respectively. AAILE was administered orally to the animals. Male Laca mice were divided into four groups: control, AAILE, DMBA/TPA and AAILE + DMBA/TPA. RESULTS: The tumors obtained in DMBA/TPA and AAILE + DMBA/TPA groups were histologically identified as SCC. Tumor induction in these groups was accompanied by raised serum carcinoembryonic antigen (CEA) levels when compared to control counterparts. Assessment of hydroxyproline levels and histochemical staining with sirius red and trichrome stain revealed an increase in collagen in tumors of DMBA/TPA group. An increase in glycosaminoglycans (GAGs) levels was also observed in DMBA/TPA group as made evident by biochemical studies and histochemical staining using mucicarmine and alcian blue-periodic acid schiff’s stain. Administration of AAILE to DMBA/TPA treated animals caused a decrease in collagen and GAG levels along with a decrease in serum CEA levels. CONCLUSION: Skin tumors exhibited altered presence of ECM components which is indicative of a modified ECM. AAILE administration antagonised tumor associated ECM alterations which may be contributing to its chemopreventive activity as reported previously.
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spelling pubmed-81167212021-05-18 Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract Chugh, N.A. Koul, A. J Tradit Complement Med Original Article BACKGROUND AND AIM: Although, the anticancer potential of Aqueous Azadirachta indica leaf extract (AAILE) has been robustly established against cutaneous squamous cell carcinoma (SCC) in mice, however, its ability in modulating tumor associated extra cellular matrix (ECM) is largely unknown. Therefore, the present study was conceived to explore changes in ECM during murine skin cancer and its chemoprevention by AAILE. EXPERIMENTAL PROCEDURE: Skin tumors were induced using a two-stage model of carcinogenesis employing topical application of 7,12-Dimethylbenz(a)anthracene (DMBA) and 12-O-tetradecanoyl phorbol-13-acetate (TPA) as carcinogen and promoter respectively. AAILE was administered orally to the animals. Male Laca mice were divided into four groups: control, AAILE, DMBA/TPA and AAILE + DMBA/TPA. RESULTS: The tumors obtained in DMBA/TPA and AAILE + DMBA/TPA groups were histologically identified as SCC. Tumor induction in these groups was accompanied by raised serum carcinoembryonic antigen (CEA) levels when compared to control counterparts. Assessment of hydroxyproline levels and histochemical staining with sirius red and trichrome stain revealed an increase in collagen in tumors of DMBA/TPA group. An increase in glycosaminoglycans (GAGs) levels was also observed in DMBA/TPA group as made evident by biochemical studies and histochemical staining using mucicarmine and alcian blue-periodic acid schiff’s stain. Administration of AAILE to DMBA/TPA treated animals caused a decrease in collagen and GAG levels along with a decrease in serum CEA levels. CONCLUSION: Skin tumors exhibited altered presence of ECM components which is indicative of a modified ECM. AAILE administration antagonised tumor associated ECM alterations which may be contributing to its chemopreventive activity as reported previously. Elsevier 2020-03-29 /pmc/articles/PMC8116721/ /pubmed/34012866 http://dx.doi.org/10.1016/j.jtcme.2020.03.006 Text en © 2020 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chugh, N.A.
Koul, A.
Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract
title Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract
title_full Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract
title_fullStr Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract
title_full_unstemmed Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract
title_short Altered presence of extra cellular matrix components in murine skin cancer: Modulation by Azadirachta indica leaf extract
title_sort altered presence of extra cellular matrix components in murine skin cancer: modulation by azadirachta indica leaf extract
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116721/
https://www.ncbi.nlm.nih.gov/pubmed/34012866
http://dx.doi.org/10.1016/j.jtcme.2020.03.006
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