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      New insights into molecular signaling pathways and current advancements in prostate cancer diagnostics & therapeutics

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          Abstract

          Prostate adenocarcinoma accounts for more than 20% of deaths among males due to cancer. It is the fifth-leading cancer diagnosed in males across the globe. The mortality rate is quite high due to prostate cancer. Despite the fact that advancements in diagnostics and therapeutics have been made, there is a lack of effective drugs. Metabolic pathways are altered due to the triggering of androgen receptor (AR) signaling pathways, and elevated levels of dihydrotestosterone are produced due to defects in AR signaling that accelerate the growth of prostate cancer cells. Further, PI3K/AKT/mTOR pathways interact with AR signaling pathway and act as precursors to promote prostate cancer. Prostate cancer therapy has been classified into luminal A, luminal B, and basal subtypes. Therapeutic drugs inhibiting dihydrotestosterone and PI3K have shown to give promising results to combat prostate cancer. Many second-generation Androgen receptor signaling antagonists are given either as single agent or with the combination of other drugs. In order to develop a cure for metastasized prostate cancer cells, Androgen deprivation therapy (ADT) is applied by using surgical or chemical methods. In many cases, Prostatectomy or local radiotherapy are used to control metastasized prostate cancer. However, it has been observed that after 1.5 years to 2 years of Prostatectomy or castration, there is reoccurrence of prostate cancer and high incidence of castration resistant prostate cancer is seen in population undergone ADT. It has been observed that Androgen derivation therapy combined with drugs like abiraterone acetate or docetaxel improve overall survival rate in metastatic hormone sensitive prostate cancer (mHSPC) patients. Scientific investigations have revealed that drugs inhibiting poly ADP Ribose polymerase (PARP) are showing promising results in clinical trials in the prostate cancer population with mCRPC and DNA repair abnormalities. Recently, RISUG adv (reversible inhibition of sperm under guidance) has shown significant results against prostate cancer cell lines and MTT assay has validated substantial effects of this drug against PC3 cell lines. Current review paper highlights the advancements in prostate cancer therapeutics and new drug molecules against prostate cancer. It will provide detailed insights on the signaling pathways which need to be targeted to combat metastasized prostate cancer and castration resistant prostate cancer.

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          Most cited references159

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          Mechanisms of receptor tyrosine kinase activation in cancer

          Receptor tyrosine kinases (RTKs) play an important role in a variety of cellular processes including growth, motility, differentiation, and metabolism. As such, dysregulation of RTK signaling leads to an assortment of human diseases, most notably, cancers. Recent large-scale genomic studies have revealed the presence of various alterations in the genes encoding RTKs such as EGFR, HER2/ErbB2, and MET, amongst many others. Abnormal RTK activation in human cancers is mediated by four principal mechanisms: gain-of-function mutations, genomic amplification, chromosomal rearrangements, and / or autocrine activation. In this manuscript, we review the processes whereby RTKs are activated under normal physiological conditions and discuss several mechanisms whereby RTKs can be aberrantly activated in human cancers. Understanding of these mechanisms has important implications for selection of anti-cancer therapies.
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            Treatment landscape of triple-negative breast cancer — expanded options, evolving needs

            Tumour heterogeneity and a long-standing paucity of effective therapies other than chemotherapy have contributed to triple-negative breast cancer (TNBC) being the subtype with the least favourable outcomes. In the past few years, advances in omics technologies have shed light on the relevance of the TNBC microenvironment heterogeneity, unveiling a close dynamic relationship with cancer cell features. An improved understanding of tumour-immune system co-evolution supports the need to adopt a more comprehensive view of TNBC as an ecosystem that encompasses the intrinsic and extrinsic features of cancer cells. This new appreciation of the biology of TNBC has already led to the development of novel targeted agents, including PARP inhibitors, antibody-drug conjugates and immune-checkpoint inhibitors, which are revolutionizing the therapeutic landscape and providing new opportunities both for patients with early-stage TNBC and for those with advanced-stage disease. The current therapeutic scenario is only the tip of the iceberg, as hundreds of new compounds and combinations are in development. The translation of these experimental therapies into clinical benefit is a welcome and ongoing challenge. In this Review, we describe the current and upcoming therapeutic landscape of TNBC and discuss how an integrated view of the TNBC ecosystem can define different levels of risk and provide improved opportunities for tailoring treatment.
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              Prostate-specific deletion of the murine Pten tumor suppressor gene leads to metastatic prostate cancer.

              The murine Pten prostate cancer model described in this study recapitulates the disease progression seen in humans: initiation of prostate cancer with prostatic intraepithelial neoplasia (PIN), followed by progression to invasive adenocarcinoma, and subsequent metastasis with defined kinetics. Furthermore, while Pten null prostate cancers regress after androgen ablation, they are capable of proliferating in the absence of androgen. Global assessment of molecular changes caused by homozygous Pten deletion identified key genes known to be relevant to human prostate cancer, including those "signature" genes associated with human cancer metastasis. This murine prostate cancer model provides a unique tool for both exploring the molecular mechanism underlying prostate cancer and for development of new targeted therapies.
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                Author and article information

                Contributors
                Journal
                Front Oncol
                Front Oncol
                Front. Oncol.
                Frontiers in Oncology
                Frontiers Media S.A.
                2234-943X
                17 August 2023
                2023
                : 13
                : 1193736
                Affiliations
                [1] 1 Department of Biotechnology, Graphic Era (Deemed to be University) , Dehradun, Uttarakhand, India
                [2] 2 Department of Chemistry, Akshara First Grade College , Bengaluru, India
                [3] 3 GenLab Biosolutions Private Limited , Bangalore, Karnataka, India
                [4] 4 Department of Biomedical Sciences, School of Life Sciences, Anglia Ruskin University , Cambridge, United Kingdom
                [5] 5 School of Health Sciences, Faculty of Biology, Medicine and Health, The University of Manchester , Manchester, United Kingdom
                [6] 6 Solution Chemistry of Advanced Materials and Technologies (SCAMT) Institute, ITMO University , St. Petersburg, Russia
                [7] 7 Department of Food Science and Technology, Graphic Era Deemed to be University , Dehradun, Uttarakhand, India
                [8] 8 Department of Biotechnology, School of Engineering and Technology, Sharda University , Greater Noida, India
                [9] 9 Department of Biotechnology Engineering and Food Technology, Chandigarh University , Mohali, India
                [10] 10 Department of Biotechnology, School of Applied & Life Sciences (SALS), Uttaranchal University , Dehradun, India
                Author notes

                Edited by: Qing Kay Li, Johns Hopkins Medicine, United States

                Reviewed by: Rintu Thomas, Baylor College of Medicine, United States; Xuxu Gou, University of California, San Francisco, United States; Marzia Di Donato, University of Campania Luigi Vanvitelli, Italy

                Article
                10.3389/fonc.2023.1193736
                10469924
                37664036
                854d458e-9795-4eae-a41c-f96d7a8a8a6e
                Copyright © 2023 Thakur, Quazi, Naik, Jha and Singh

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 25 March 2023
                : 18 July 2023
                Page count
                Figures: 3, Tables: 2, Equations: 0, References: 160, Pages: 20, Words: 10724
                Funding
                SQ was responsible for funding acquisition. The APC were paid for by the University of Manchester, United Kingdom.
                Categories
                Oncology
                Review
                Custom metadata
                Molecular and Cellular Oncology

                Oncology & Radiotherapy
                prostate cancer,androgen deprivation therapy,castration resistant prostate cancer,risug adv,poly adp ribose polymerase,ar signaling,pi3k

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