ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation

The bacterial antigen, lipopolysaccharide (LPS) and disruptions in calcium channels are independently known to influence oral cancer progression. Previously, we found that bacterial antigens, LPS and lipoteichoic acid (LTA) act as confounders during the action of capsaicin on Cal 27 oral cancer prol...

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Autores principales: Rajdeep Chakraborty, Honghua Hu, Charbel Darido, Karen Vickery, Shoba Ranganathan
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/b02dc11edf2f412eacdd208973f363d8
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spelling oai:doaj.org-article:b02dc11edf2f412eacdd208973f363d82021-11-25T17:57:49ZML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation10.3390/ijms2222125591422-00671661-6596https://doaj.org/article/b02dc11edf2f412eacdd208973f363d82021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/22/12559https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067The bacterial antigen, lipopolysaccharide (LPS) and disruptions in calcium channels are independently known to influence oral cancer progression. Previously, we found that bacterial antigens, LPS and lipoteichoic acid (LTA) act as confounders during the action of capsaicin on Cal 27 oral cancer proliferation. As calcium channel drugs may affect oral cancer cell proliferation, we investigated the effect of ML218 HCl, a T-type voltage-gated calcium channel blocker, on the proliferation of Cal 27 oral cancer cells. We hypothesized that ML218 HCl could effectively reduce LPS-induced oral cancer cell proliferation. LPS and LTA antigens were added to Cal 27 oral cancer cells either prior to and/or concurrently with ML218 HCl treatment, and the efficacy of the treatment was evaluated by measuring Cal 27 proliferation, cell death and apoptosis. ML218 HCl inhibited oral cancer cell proliferation, increased apoptosis and cell death, but their efficacy was significantly reduced in the presence of bacterial antigens. ML218 HCl proved more effective than capsaicin in reducing bacterial antigen-induced Cal 27 oral cancer cell proliferation. Our results also suggest an interplay of proliferation factors during the bacterial antigens and calcium channel drug interaction in Cal 27. Bacterial antigen reduction of drug efficacy should be considered for developing newer pharmacological agents or testing the efficacy of the existing oral cancer chemotherapeutic agents. Finally, voltage gated calcium channel drugs should be considered for future oral cancer research.Rajdeep ChakrabortyHonghua HuCharbel DaridoKaren VickeryShoba RanganathanMDPI AGarticlelipopolysaccharidelipoteichoic acidoral cancerML218 HClcapsaicinproliferationBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 12559, p 12559 (2021)
institution DOAJ
collection DOAJ
language EN
topic lipopolysaccharide
lipoteichoic acid
oral cancer
ML218 HCl
capsaicin
proliferation
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle lipopolysaccharide
lipoteichoic acid
oral cancer
ML218 HCl
capsaicin
proliferation
Biology (General)
QH301-705.5
Chemistry
QD1-999
Rajdeep Chakraborty
Honghua Hu
Charbel Darido
Karen Vickery
Shoba Ranganathan
ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation
description The bacterial antigen, lipopolysaccharide (LPS) and disruptions in calcium channels are independently known to influence oral cancer progression. Previously, we found that bacterial antigens, LPS and lipoteichoic acid (LTA) act as confounders during the action of capsaicin on Cal 27 oral cancer proliferation. As calcium channel drugs may affect oral cancer cell proliferation, we investigated the effect of ML218 HCl, a T-type voltage-gated calcium channel blocker, on the proliferation of Cal 27 oral cancer cells. We hypothesized that ML218 HCl could effectively reduce LPS-induced oral cancer cell proliferation. LPS and LTA antigens were added to Cal 27 oral cancer cells either prior to and/or concurrently with ML218 HCl treatment, and the efficacy of the treatment was evaluated by measuring Cal 27 proliferation, cell death and apoptosis. ML218 HCl inhibited oral cancer cell proliferation, increased apoptosis and cell death, but their efficacy was significantly reduced in the presence of bacterial antigens. ML218 HCl proved more effective than capsaicin in reducing bacterial antigen-induced Cal 27 oral cancer cell proliferation. Our results also suggest an interplay of proliferation factors during the bacterial antigens and calcium channel drug interaction in Cal 27. Bacterial antigen reduction of drug efficacy should be considered for developing newer pharmacological agents or testing the efficacy of the existing oral cancer chemotherapeutic agents. Finally, voltage gated calcium channel drugs should be considered for future oral cancer research.
format article
author Rajdeep Chakraborty
Honghua Hu
Charbel Darido
Karen Vickery
Shoba Ranganathan
author_facet Rajdeep Chakraborty
Honghua Hu
Charbel Darido
Karen Vickery
Shoba Ranganathan
author_sort Rajdeep Chakraborty
title ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation
title_short ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation
title_full ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation
title_fullStr ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation
title_full_unstemmed ML218 HCl Is More Efficient Than Capsaicin in Inhibiting Bacterial Antigen-Induced Cal 27 Oral Cancer Cell Proliferation
title_sort ml218 hcl is more efficient than capsaicin in inhibiting bacterial antigen-induced cal 27 oral cancer cell proliferation
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/b02dc11edf2f412eacdd208973f363d8
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AT honghuahu ml218hclismoreefficientthancapsaicinininhibitingbacterialantigeninducedcal27oralcancercellproliferation
AT charbeldarido ml218hclismoreefficientthancapsaicinininhibitingbacterialantigeninducedcal27oralcancercellproliferation
AT karenvickery ml218hclismoreefficientthancapsaicinininhibitingbacterialantigeninducedcal27oralcancercellproliferation
AT shobaranganathan ml218hclismoreefficientthancapsaicinininhibitingbacterialantigeninducedcal27oralcancercellproliferation
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