The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma

Uveal melanoma (UM) is the most common primary intraocular cancer in the adult population. Recent studies suggested that the NLRP3 inflammasome could be a therapeutic target for cutaneous melanoma (CM), but the role of NLRP3 in UM remains unknown. Here, we analyzed the NLRP3‐IL‐1β axis in 5 UM and 4...

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Main Authors: Victor S. M. C. Correa, Nikolaos E. Efstathiou, Dimitrios P. Ntentakis, Zhen Yu, Toshio Narimatsu, Evangelos Gragoudas, Ivana K. Kim, Demetrios G. Vavvas
Format: Article
Language:English
Published: Wiley 2023-03-01
Series:FEBS Open Bio
Subjects:
Online Access:https://doi.org/10.1002/2211-5463.13566
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author Victor S. M. C. Correa
Nikolaos E. Efstathiou
Dimitrios P. Ntentakis
Zhen Yu
Toshio Narimatsu
Evangelos Gragoudas
Ivana K. Kim
Demetrios G. Vavvas
author_facet Victor S. M. C. Correa
Nikolaos E. Efstathiou
Dimitrios P. Ntentakis
Zhen Yu
Toshio Narimatsu
Evangelos Gragoudas
Ivana K. Kim
Demetrios G. Vavvas
author_sort Victor S. M. C. Correa
collection DOAJ
description Uveal melanoma (UM) is the most common primary intraocular cancer in the adult population. Recent studies suggested that the NLRP3 inflammasome could be a therapeutic target for cutaneous melanoma (CM), but the role of NLRP3 in UM remains unknown. Here, we analyzed the NLRP3‐IL‐1β axis in 5 UM and 4 CM cell lines. Expression of NLRP3 mRNA in UM and CM was low, and expression in UM was lower than in CM (P < 0.001). NLRP3 protein levels were below detection limit for all cell lines. UM exhibited lower baseline IL‐1β secretion than CM, especially when compared to the Hs294t cell line (P < 0.05). Bioinformatic analysis of human tumor samples showed that UM has significantly lower expression of NLRP3 and IL‐1β compared with CM. In conclusion, our work shows evidence of extremely low NLRP3 expression and IL‐1β secretion by melanoma cells and highlight differences between CM and UM.
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spelling doaj.art-2b15d55188dc4325a2431a9d3f7849642023-03-07T09:42:22ZengWileyFEBS Open Bio2211-54632023-03-0113354555510.1002/2211-5463.13566The NLRP3 inflammasome – interleukin 1β axis in uveal melanomaVictor S. M. C. Correa0Nikolaos E. Efstathiou1Dimitrios P. Ntentakis2Zhen Yu3Toshio Narimatsu4Evangelos Gragoudas5Ivana K. Kim6Demetrios G. Vavvas7Retina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USARetina Service, Ines and Fred Yeatts Retina Research Laboratory, Angiogenesis Laboratory, Department of Ophthalmology Massachusetts Eye and Ear, Harvard Medical School Boston MA USAUveal melanoma (UM) is the most common primary intraocular cancer in the adult population. Recent studies suggested that the NLRP3 inflammasome could be a therapeutic target for cutaneous melanoma (CM), but the role of NLRP3 in UM remains unknown. Here, we analyzed the NLRP3‐IL‐1β axis in 5 UM and 4 CM cell lines. Expression of NLRP3 mRNA in UM and CM was low, and expression in UM was lower than in CM (P < 0.001). NLRP3 protein levels were below detection limit for all cell lines. UM exhibited lower baseline IL‐1β secretion than CM, especially when compared to the Hs294t cell line (P < 0.05). Bioinformatic analysis of human tumor samples showed that UM has significantly lower expression of NLRP3 and IL‐1β compared with CM. In conclusion, our work shows evidence of extremely low NLRP3 expression and IL‐1β secretion by melanoma cells and highlight differences between CM and UM.https://doi.org/10.1002/2211-5463.13566IL‐1inflammasomemelanomaNLRP3skinuveal
spellingShingle Victor S. M. C. Correa
Nikolaos E. Efstathiou
Dimitrios P. Ntentakis
Zhen Yu
Toshio Narimatsu
Evangelos Gragoudas
Ivana K. Kim
Demetrios G. Vavvas
The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma
FEBS Open Bio
IL‐1
inflammasome
melanoma
NLRP3
skin
uveal
title The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma
title_full The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma
title_fullStr The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma
title_full_unstemmed The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma
title_short The NLRP3 inflammasome – interleukin 1β axis in uveal melanoma
title_sort nlrp3 inflammasome interleukin 1β axis in uveal melanoma
topic IL‐1
inflammasome
melanoma
NLRP3
skin
uveal
url https://doi.org/10.1002/2211-5463.13566
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