Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer

Background: Prostate cancer is the second most frequently diagnosed malignancy worldwide. Here, the cytotoxic and antimetastatic effects of a new HDAC6/8 inhibitor, LASSBio-1911, and a new dual-PI3K/HDAC6 inhibitor, LASSBio-2208, were evaluated against PC3 prostate cancer cell line. Methods: A MTT a...

Full description

Bibliographic Details
Main Authors: Fabiana Sélos Guerra, Daniel Alencar Rodrigues, Carlos Alberto Manssour Fraga, Patricia Dias Fernandes
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/14/5/387
id doaj-4085331ebd6b4373b8834c8d13d55de8
record_format Article
spelling doaj-4085331ebd6b4373b8834c8d13d55de82021-04-21T23:01:43ZengMDPI AGPharmaceuticals1424-82472021-04-011438738710.3390/ph14050387Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate CancerFabiana Sélos Guerra0Daniel Alencar Rodrigues1Carlos Alberto Manssour Fraga2Patricia Dias Fernandes3Laboratório de Farmacologia da Dor e da Inflamação, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, BrazilLaboratório de Avaliação e Síntese de Substâncias Bioativas (LASSBio), Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, BrazilLaboratório de Avaliação e Síntese de Substâncias Bioativas (LASSBio), Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, BrazilLaboratório de Farmacologia da Dor e da Inflamação, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, BrazilBackground: Prostate cancer is the second most frequently diagnosed malignancy worldwide. Here, the cytotoxic and antimetastatic effects of a new HDAC6/8 inhibitor, LASSBio-1911, and a new dual-PI3K/HDAC6 inhibitor, LASSBio-2208, were evaluated against PC3 prostate cancer cell line. Methods: A MTT assay was used to assess the cell viability. Annexin V/propidium iodide (PI) was used to detect apoptotic cell death and to analyze the cell cycle distribution. Interleukin 6 (IL-6) levels were measured by ELISA. A cell scratch assay was performed to assess cell migration, and the expression of proteins was estimated by Western blotting. Results: LASSBio-1911 and LASSBio-2208 exert cytotoxic effects against PC3 cells. However, LASSBio-2208 was demonstrated to be more potent than LASSBio-1911. The apoptosis assays showed that both compounds trigger apoptotic processes and cause the arrest of cells in the G2/M phase of the cell cycle. The Western blot analysis revealed that LASSBio-2208 significantly decreased the expression of p-JNK and JAK2. However, both compounds reduced the expression of p-STAT3, IL-6 secretion, and cell migration. Conclusions: LASSBio-1911 and LASSBio-2208 demonstrated significant activity in reducing cell viability and migration. These compounds can be further used as prototypes for the development of new potential anticancer alternative treatments.https://www.mdpi.com/1424-8247/14/5/387cancerprostate cancerPI3KHDAC6apoptosiscell cycle
collection DOAJ
language English
format Article
sources DOAJ
author Fabiana Sélos Guerra
Daniel Alencar Rodrigues
Carlos Alberto Manssour Fraga
Patricia Dias Fernandes
spellingShingle Fabiana Sélos Guerra
Daniel Alencar Rodrigues
Carlos Alberto Manssour Fraga
Patricia Dias Fernandes
Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer
Pharmaceuticals
cancer
prostate cancer
PI3K
HDAC6
apoptosis
cell cycle
author_facet Fabiana Sélos Guerra
Daniel Alencar Rodrigues
Carlos Alberto Manssour Fraga
Patricia Dias Fernandes
author_sort Fabiana Sélos Guerra
title Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer
title_short Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer
title_full Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer
title_fullStr Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer
title_full_unstemmed Novel Single Inhibitor of HDAC6/8 and Dual Inhibitor of PI3K/HDAC6 as Potential Alternative Treatments for Prostate Cancer
title_sort novel single inhibitor of hdac6/8 and dual inhibitor of pi3k/hdac6 as potential alternative treatments for prostate cancer
publisher MDPI AG
series Pharmaceuticals
issn 1424-8247
publishDate 2021-04-01
description Background: Prostate cancer is the second most frequently diagnosed malignancy worldwide. Here, the cytotoxic and antimetastatic effects of a new HDAC6/8 inhibitor, LASSBio-1911, and a new dual-PI3K/HDAC6 inhibitor, LASSBio-2208, were evaluated against PC3 prostate cancer cell line. Methods: A MTT assay was used to assess the cell viability. Annexin V/propidium iodide (PI) was used to detect apoptotic cell death and to analyze the cell cycle distribution. Interleukin 6 (IL-6) levels were measured by ELISA. A cell scratch assay was performed to assess cell migration, and the expression of proteins was estimated by Western blotting. Results: LASSBio-1911 and LASSBio-2208 exert cytotoxic effects against PC3 cells. However, LASSBio-2208 was demonstrated to be more potent than LASSBio-1911. The apoptosis assays showed that both compounds trigger apoptotic processes and cause the arrest of cells in the G2/M phase of the cell cycle. The Western blot analysis revealed that LASSBio-2208 significantly decreased the expression of p-JNK and JAK2. However, both compounds reduced the expression of p-STAT3, IL-6 secretion, and cell migration. Conclusions: LASSBio-1911 and LASSBio-2208 demonstrated significant activity in reducing cell viability and migration. These compounds can be further used as prototypes for the development of new potential anticancer alternative treatments.
topic cancer
prostate cancer
PI3K
HDAC6
apoptosis
cell cycle
url https://www.mdpi.com/1424-8247/14/5/387
work_keys_str_mv AT fabianaselosguerra novelsingleinhibitorofhdac68anddualinhibitorofpi3khdac6aspotentialalternativetreatmentsforprostatecancer
AT danielalencarrodrigues novelsingleinhibitorofhdac68anddualinhibitorofpi3khdac6aspotentialalternativetreatmentsforprostatecancer
AT carlosalbertomanssourfraga novelsingleinhibitorofhdac68anddualinhibitorofpi3khdac6aspotentialalternativetreatmentsforprostatecancer
AT patriciadiasfernandes novelsingleinhibitorofhdac68anddualinhibitorofpi3khdac6aspotentialalternativetreatmentsforprostatecancer
_version_ 1721515419693481984