TY - JOUR
T1 - The impact of metabolic syndrome and type 2 diabetes mellitus on prostate cancer
AU - Sousa, André P.
AU - Costa, Raquel
AU - Alves, Marco G.
AU - Soares, Raquel
AU - Baylina, Pilar
AU - Fernandes, Rúben
N1 - Funding Information:
This paper is payed by means of own recepies. RF acknowledges, on the behalf of the authors, the funding entities. This work was also supported by FCT - Fundação para a Ciência e Tecnologia (UID/BIM/04293/2013) and by grants NORTE-01-0145-FEDER-000012, SAICT-POL/24325/2016 and FEDER/02/SAICT/2020/072560.
Funding Information:
This paper is payed by means of own recepies. RF acknowledges, on the behalf of the authors, the funding entities. This work was also supported by FCT - Funda??o para a Ci?ncia e Tecnologia (UID/BIM/04293/2013) and by grants NORTE-01-0145-FEDER-000012, SAICT-POL/24325/2016 and FEDER/02/SAICT/2020/072560.
Publisher Copyright:
Copyright © 2022 Sousa, Costa, Alves, Soares, Baylina and Fernandes.
PY - 2022/3/25
Y1 - 2022/3/25
N2 - Prostate cancer (PCa) remains the second most common type of cancer in men worldwide in 2020. Despite its low death rate, the need for new therapies or prevention strategies is critical. The prostate carcinogenesis process is complex and multifactorial. PCa is caused by a variety of mutations and carcinogenic events that constitutes the disease’s multifactorial focus, capable of not only remodeling cellular activity, but also modeling metabolic pathways to allow adaptation to the nutritional requirements of the tumor, creating a propitious microenvironment. Some risk factors have been linked to the development of PCa, including Metabolic Syndrome (MetS) and Type 2 Diabetes Mellitus (T2DM). MetS is intrinsically related to PCa carcinogenic development, increasing its aggressiveness. On the other hand, T2DM has the opposite impact, although in other carcinomas its effect is similar to the MetS. Although these two metabolic disorders may share some developmental processes, such as obesity, insulin resistance, and dyslipidemia, their influence on PCa prognosis appears to have an inverse effect, which makes this a paradox. Understanding the phenomena behind this paradoxical behavior may lead to new concepts into the comprehension of the diseases, as well as to evaluate new therapeutical targets. Thus, this review aimed to evaluate the impact of metabolic disorders in PCa’s aggressiveness state and metabolism.
AB - Prostate cancer (PCa) remains the second most common type of cancer in men worldwide in 2020. Despite its low death rate, the need for new therapies or prevention strategies is critical. The prostate carcinogenesis process is complex and multifactorial. PCa is caused by a variety of mutations and carcinogenic events that constitutes the disease’s multifactorial focus, capable of not only remodeling cellular activity, but also modeling metabolic pathways to allow adaptation to the nutritional requirements of the tumor, creating a propitious microenvironment. Some risk factors have been linked to the development of PCa, including Metabolic Syndrome (MetS) and Type 2 Diabetes Mellitus (T2DM). MetS is intrinsically related to PCa carcinogenic development, increasing its aggressiveness. On the other hand, T2DM has the opposite impact, although in other carcinomas its effect is similar to the MetS. Although these two metabolic disorders may share some developmental processes, such as obesity, insulin resistance, and dyslipidemia, their influence on PCa prognosis appears to have an inverse effect, which makes this a paradox. Understanding the phenomena behind this paradoxical behavior may lead to new concepts into the comprehension of the diseases, as well as to evaluate new therapeutical targets. Thus, this review aimed to evaluate the impact of metabolic disorders in PCa’s aggressiveness state and metabolism.
KW - Cancer biology
KW - Diabetes
KW - Metabolic syndrome
KW - Metabolism
KW - Prostate cancer
KW - Signaling/signaling pathways
UR - http://www.scopus.com/inward/record.url?scp=85128412360&partnerID=8YFLogxK
U2 - 10.3389/fcell.2022.843458
DO - 10.3389/fcell.2022.843458
M3 - Review article
C2 - 35399507
AN - SCOPUS:85128412360
SN - 2296-634X
VL - 10
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 843458
ER -