A Comprehensive Review on PARP Inhibitors in Targeted Therapy for Cancers DOI Creative Commons

Mounika Guduri,

Samyuktha Kolluru,

Haritha Pasupulati

и другие.

Deleted Journal, Год журнала: 2024, Номер 19(2), С. 44 - 59

Опубликована: Авг. 9, 2024

The poly (ADP-ribose) polymerase (PARP) family of enzymes involves and regulates various cellular processes essential functions, such as apoptosis, transcription process, DNA repair. PARPs (PARP-1, PARP-2, PARP-3) are a branch familiar proteins that play crucial role in repairing damage human gene involved different cancers regulate the base excision repair (BER) pathway. As target-based drug therapy for cancer, inhibition PARP stops PARP-1 -2 from damaged mutated cancer cells, eventually, cells die. Considering limited available therapies treatment advanced recurrent cancers, inhibitors (PARPi) first approved drugs particularly target response to BRCA (BReast CAncer gene)-1/2 ovarian, pancreatic, prostate, breast cancers. Recently, six PARPi viz., olaparib, rucaparib, niraparib, talazoparib, fuzuloparib, pamiparib were monotherapy or combination with other classes anticancer agents maintenance Moreover, appears improve progression-free survival women platinum-sensitive ovarian an adjuvant conventional treatment. Importantly, use management germline BRCA1/2-associated is novel therapeutic strategy, representing successful targeted improving outcomes patients hereditary Although resistance these has been reported recently, however, strategies have employed overcome sensitivity breast, gastric, prostate

Язык: Английский

Mass Spectrometry‐Based Proteomics for Next‐Generation Precision Oncology DOI
Kuen‐Tyng Lin, Gul Muneer, Peirong Huang

и другие.

Mass Spectrometry Reviews, Год журнала: 2025, Номер unknown

Опубликована: Апрель 23, 2025

ABSTRACT Cancer is the leading cause of death worldwide characterized by patient heterogeneity and complex tumor microenvironment. While genomics‐based testing has transformed modern medicine, challenge diverse clinical outcomes highlights unmet needs for precision oncology. As functional molecules regulating cellular processes, proteins hold great promise as biomarkers drug targets. Mass spectrometry (MS)‐based proteomics illuminated molecular features cancers facilitated discovery or therapeutic targets, paving way innovative strategies that enhance personalized treatment. In this article, we introduced tools current achievements MS‐based proteomics, choice targeted MS from to validation phases, profiling sensitivity bulk samples single‐cell level tissue liquid biopsy specimens, regulatory landscape protein laboratory‐developed tests (LDTs). The challenges, success future perspectives in translating research assay into applications are also discussed. With well‐designed studies demonstrate benefits meet requirements both analytical performance, assays promising with numerous opportunities improve cancer diagnosis, treatment, monitoring.

Язык: Английский

Процитировано

0

Precision Targeting in Metastatic Prostate Cancer: Molecular Insights to Therapeutic Frontiers DOI Creative Commons
Whi‐An Kwon, Jae Young Joung

Biomolecules, Год журнала: 2025, Номер 15(5), С. 625 - 625

Опубликована: Апрель 27, 2025

Metastatic prostate cancer (mPCa) remains a significant cause of cancer-related mortality in men. Advances molecular profiling have demonstrated that the androgen receptor (AR) axis, DNA damage repair pathways, and PI3K/AKT/mTOR pathway are critical drivers disease progression therapeutic resistance. Despite established benefits hormone therapy, chemotherapy, bone-targeting agents, mPCa commonly becomes treatment-resistant. Recent breakthroughs highlighted importance identifying actionable genetic alterations, such as BRCA2 or ATM defects, render tumors sensitive to poly-ADP ribose polymerase (PARP) inhibitors. Parallel efforts refined imaging—particularly prostate-specific membrane antigen (PSMA) positron emission tomography-computed tomography—to detect localize metastatic lesions with high sensitivity, thereby guiding patient selection for PSMA-targeted radioligand therapies. Multi-omics innovations, including liquid biopsy technologies, enable real-time tracking emergent AR splice variants reversion mutations, supporting adaptive therapy paradigms. Nonetheless, complexity necessitates combination strategies, pairing inhibition PI3K/AKT blockade PARP inhibitors, inhibit tumor plasticity. Immuno-oncological approaches remain challenging unselected patients; however, subsets mismatch deficiency neuroendocrine phenotypes may benefit from immune checkpoint targeted epigenetic interventions. We present these pivotal advances, discuss how biomarker-guided integrative treatments can improve management.

Язык: Английский

Процитировано

0

Biomarker validation: challenges and regulatory perspectives DOI
Bindiya Chauhan, Bhuvnesh Kumar Singh,

Tuhin James Paul

и другие.

Elsevier eBooks, Год журнала: 2025, Номер unknown, С. 149 - 176

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Poly-ADP Ribose Polymerase Inhibitors and Combinations in Metastatic Prostate Cancer DOI
Obada Ababneh, Rana R. McKay

Advances in Oncology, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Characteristics of Patients with Newly Diagnosed High-Grade Advanced Ovarian, Fallopian Tube, and Primary Peritoneal Cancer in 2018–2023 and the Impact of Molecular Diagnostics on Chemotherapy in Clinical Practice DOI Creative Commons
Sonja Millert-Kalińska, Małgorzata Stawicka-Niełacna,

Lidia Tomczak

и другие.

Biomedicines, Год журнала: 2025, Номер 13(2), С. 483 - 483

Опубликована: Фев. 15, 2025

Background: High-grade advanced ovarian, fallopian tube, and primary peritoneal (HGAOC) cancers require both surgical systemic treatment. The introduction of polyADP-ribose polymerase inhibitors (PARPis) has significantly improved outcomes. This study presents an analysis HGAOC patients treated at a single center, following updated guidelines. Methods: We observed 437 women newly diagnosed with the Department Gynecological Oncology between January 2018 December 2023. Results: Since November 2022, first-line treatment included bevacizumab PARPi, regardless residual disease post-cytoreductive surgery. In BRCA1/2-mutated non-mutated groups, PARPi-based regimens increased after May 2021 (p < 0.01). Recurrence number emerged as strong prognostic factor for survival 0.001), each recurrence raising mortality risk by 80%. Median was 21 months paclitaxel + platinum derivatives (PC), 27 PC (BEV), 30 BEV PARPi. Conclusions: rapid adoption modern therapies our center aligned strategies HRD status global standards. However, variations in financial regulations drug accessibility persist across countries. Despite these challenges, physicians should prioritize most effective available.

Язык: Английский

Процитировано

0

Advances in DNA Damage Detection: Current Progress, Challenges, and Future Directions DOI Creative Commons
Heeseok Kang,

Hyung Joon Park,

Jieun Kang

и другие.

TrAC Trends in Analytical Chemistry, Год журнала: 2025, Номер unknown, С. 118246 - 118246

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Biomarkers DOI

Pradip Nair,

Bindhu Omana Sukumaran,

Sayeeda Mussavira

и другие.

Опубликована: Янв. 1, 2025

Процитировано

0

The Role of Multi-Omics in Breast Cancer Diagnosis and Research DOI Open Access
Klaudia Kulczyńska,

Michalina Kliber

Letters in Oncology Science, Год журнала: 2025, Номер 22(1)

Опубликована: Май 5, 2025

Breast cancer is the most common malignancy among women and a leading cause of cancer-related mortality. Despite significant advances in detection treatment, its molecular heterogeneity poses challenges achieving accurate diagnosis personalized therapies. Traditional diagnostic methods, based primarily on histopathology genomics, fail to capture full complexity disease. In response, multi-omics approaches, integrating transcriptomics, proteomics, metabolomics, are emerging as powerful tools for comprehensive profiling. These advanced methodologies enable identification novel biomarkers, improve accuracy, facilitate patient stratification tailored treatments. This review explores role breast diagnosis, emphasizing recent technological advancements key findings that enhance early detection, prognosis, treatment strategies. By providing more complete picture, paving way precision medicine, offering potential effective

Язык: Английский

Процитировано

0

Overexpression of ABCC1 and ABCG2 confers resistance to talazoparib, a poly (ADP-Ribose) polymerase inhibitor DOI

Qiu‐Xu Teng,

Zi‐Ning Lei, Jing‐Quan Wang

и другие.

Drug Resistance Updates, Год журнала: 2023, Номер 73, С. 101028 - 101028

Опубликована: Ноя. 29, 2023

Язык: Английский

Процитировано

8

Navigating ethical challenges of integrating genomic medicine into clinical practice: Maximising beneficence in precision oncology DOI Creative Commons
Maritha J. Kotze,

K.A. Grant,

Nerina C. van der Merwe

и другие.

South African Journal of Bioethics and Law, Год журнала: 2024, Номер unknown, С. e2071 - e2071

Опубликована: Апрель 23, 2024

The development of gene expression profiling and next-generation sequencing technologies have steered oncogenomics to the forefront precision medicine. This created a need for harmonious cooperation between clinicians researchers increase access oncology, despite multiple implementation challenges being encountered. aim is apply personalised treatment strategies early in cancer management, targeting tumour subtypes actionable variants within individual’s broader clinical risk profile wellbeing. A knowledge-generating database linked South African Medical Research Council’s Genomic Centre has been application medicine, using an integrated service research approach. Insights gained from patient experiences related heterogeneity, targeted therapies incidental findings pathogenic germline DNA, provided practice-changing evidence cost-minimisation pathology-supported genetic testing strategy. Integrating care with genomic through data sharing advances medicine maximises oncology benefits.

Язык: Английский

Процитировано

3