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In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses
Tumor acidity is the key metabolic feature promoting cancer progression and is modulated by pH regulators on a cancer cell's surface that pump out excess protons/lactic acid for cancer cell survival. Neutralizing tumor acidity improves the therapeutic efficacy of current treatments including im...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530789/ https://www.ncbi.nlm.nih.gov/pubmed/32797726 http://dx.doi.org/10.1002/1878-0261.12782 |
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author | Kulshrestha, Arpita Katara, Gajendra K. Ibrahim, Safaa A. Riehl, Valerie E. Schneiderman, Sylvia Bilal, Mahmood Young, Alexandria N. Levine, Shayna Fleetwood, Sara Dolan, James Gilman‐Sachs, Alice Beaman, Kenneth D. |
author_facet | Kulshrestha, Arpita Katara, Gajendra K. Ibrahim, Safaa A. Riehl, Valerie E. Schneiderman, Sylvia Bilal, Mahmood Young, Alexandria N. Levine, Shayna Fleetwood, Sara Dolan, James Gilman‐Sachs, Alice Beaman, Kenneth D. |
author_sort | Kulshrestha, Arpita |
collection | PubMed |
description | Tumor acidity is the key metabolic feature promoting cancer progression and is modulated by pH regulators on a cancer cell's surface that pump out excess protons/lactic acid for cancer cell survival. Neutralizing tumor acidity improves the therapeutic efficacy of current treatments including immunotherapies. Vacuolar‐ATPase (V‐ATPase) proton pumps encompass unique plasma membrane‐associated subunit isoforms, making this molecule an important target for anticancer therapy. Here, we examined the in vivo therapeutic efficacy of an antibody (a2v‐mAB) targeting specific V‐ATPase‐‘V0a2’ surface isoform in controlling ovarian tumor growth. In vitro a2v‐mAb treatment inhibited the proton pump activity in ovarian cancer (OVCA) cells. In vivo intraperitoneal a2v‐mAb treatment drastically delayed ovarian tumor growth with no measurable in vivo toxicity in a transplant tumor model. To explore the possible mechanism causing delayed tumor growth, histochemical analysis of the a2v‐mAb‐treated tumor tissues displayed high immune cell infiltration (M1‐macrophages, neutrophils, CD103(+) cells, and NK cells) and an enhanced antitumor response (iNOS, IFN‐y, IL‐1α) compared to control. There was marked decrease in CA‐125‐positive cancer cells and an enhanced active caspase‐3 expression in a2v‐mAb‐treated tumors. RNA‐seq analysis of a2v‐mAb tumor tissues further revealed upregulation of apoptosis‐related and toll‐like receptor pathway‐related genes. Indirect coculture of a2v‐mAb‐treated OVCA cells with human PBMCs in an unbuffered medium led to an enhanced gene expression of antitumor molecules IFN‐y, IL‐17, and IL‐12‐A in PBMCs, further validating the in vivo antitumor responses. In conclusion, V‐ATPase inhibition using a monoclonal antibody directed against the V0a2 isoform increases antitumor immune responses and could therefore constitute an effective treatment strategy in OVCA. |
format | Online Article Text |
id | pubmed-7530789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75307892020-10-05 In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses Kulshrestha, Arpita Katara, Gajendra K. Ibrahim, Safaa A. Riehl, Valerie E. Schneiderman, Sylvia Bilal, Mahmood Young, Alexandria N. Levine, Shayna Fleetwood, Sara Dolan, James Gilman‐Sachs, Alice Beaman, Kenneth D. Mol Oncol Research Articsles Tumor acidity is the key metabolic feature promoting cancer progression and is modulated by pH regulators on a cancer cell's surface that pump out excess protons/lactic acid for cancer cell survival. Neutralizing tumor acidity improves the therapeutic efficacy of current treatments including immunotherapies. Vacuolar‐ATPase (V‐ATPase) proton pumps encompass unique plasma membrane‐associated subunit isoforms, making this molecule an important target for anticancer therapy. Here, we examined the in vivo therapeutic efficacy of an antibody (a2v‐mAB) targeting specific V‐ATPase‐‘V0a2’ surface isoform in controlling ovarian tumor growth. In vitro a2v‐mAb treatment inhibited the proton pump activity in ovarian cancer (OVCA) cells. In vivo intraperitoneal a2v‐mAb treatment drastically delayed ovarian tumor growth with no measurable in vivo toxicity in a transplant tumor model. To explore the possible mechanism causing delayed tumor growth, histochemical analysis of the a2v‐mAb‐treated tumor tissues displayed high immune cell infiltration (M1‐macrophages, neutrophils, CD103(+) cells, and NK cells) and an enhanced antitumor response (iNOS, IFN‐y, IL‐1α) compared to control. There was marked decrease in CA‐125‐positive cancer cells and an enhanced active caspase‐3 expression in a2v‐mAb‐treated tumors. RNA‐seq analysis of a2v‐mAb tumor tissues further revealed upregulation of apoptosis‐related and toll‐like receptor pathway‐related genes. Indirect coculture of a2v‐mAb‐treated OVCA cells with human PBMCs in an unbuffered medium led to an enhanced gene expression of antitumor molecules IFN‐y, IL‐17, and IL‐12‐A in PBMCs, further validating the in vivo antitumor responses. In conclusion, V‐ATPase inhibition using a monoclonal antibody directed against the V0a2 isoform increases antitumor immune responses and could therefore constitute an effective treatment strategy in OVCA. John Wiley and Sons Inc. 2020-09-10 2020-10 /pmc/articles/PMC7530789/ /pubmed/32797726 http://dx.doi.org/10.1002/1878-0261.12782 Text en © 2020 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articsles Kulshrestha, Arpita Katara, Gajendra K. Ibrahim, Safaa A. Riehl, Valerie E. Schneiderman, Sylvia Bilal, Mahmood Young, Alexandria N. Levine, Shayna Fleetwood, Sara Dolan, James Gilman‐Sachs, Alice Beaman, Kenneth D. In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
title |
In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
title_full |
In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
title_fullStr |
In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
title_full_unstemmed |
In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
title_short |
In vivo anti‐V‐ATPase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
title_sort | in vivo anti‐v‐atpase antibody treatment delays ovarian tumor growth by increasing antitumor immune responses |
topic | Research Articsles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530789/ https://www.ncbi.nlm.nih.gov/pubmed/32797726 http://dx.doi.org/10.1002/1878-0261.12782 |
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