Investigation of CST7 and hsa-miR-4793-5p gene expression in breast cancer DOI Creative Commons
Niloufar Sadat Kalaki, Mozhgan Ahmadzadeh,

Mojtaba Dehghan

et al.

Biochemistry and Biophysics Reports, Journal Year: 2024, Volume and Issue: 40, P. 101863 - 101863

Published: Nov. 1, 2024

Language: Английский

Beyond genetics: Exploring the role of epigenetic alterations in breast cancer DOI Creative Commons

Kirti S. Prabhu,

Hana Q. Sadida,

Shilpa Kuttikrishnan

et al.

Pathology - Research and Practice, Journal Year: 2024, Volume and Issue: 254, P. 155174 - 155174

Published: Jan. 26, 2024

Breast cancer remains a major global health challenge. Its rising incidence is attributed to factors such as delayed diagnosis, the complexity of its subtypes, and increasing drug resistance, all contributing less-than-ideal patient outcomes. Central progression breast are epigenetic aberrations, which significantly contribute resistance emergence stem cell traits. These include alterations in DNA methylation, histone modifications, expression non-coding RNAs. Understanding these changes crucial for developing advanced management strategies despite their complexity. Investigating modifications offers potential novel diagnostic markers, more accurate prognostic indicators, identification reliable predictors treatment response. This could lead development new targeted therapies. However, this requires sustained, focused research efforts navigate challenges understanding carcinogenesis underpinnings. A deeper mechanisms can revolutionize personalized medicine. significant improvements care, including early detection, precise disease stratification, effective options.

Language: Английский

Citations

17

Molecular Insights on Signaling Cascades in Breast Cancer: A Comprehensive Review DOI Open Access
Venketesh K. Panda,

Barnalee Mishra,

Samikshya Mahapatra

et al.

Cancers, Journal Year: 2025, Volume and Issue: 17(2), P. 234 - 234

Published: Jan. 13, 2025

The complex signaling network within the breast tumor microenvironment is crucial for its growth, metastasis, angiogenesis, therapy escape, stem cell maintenance, and immunomodulation. An array of secretory factors their receptors activate downstream cascades regulating cancer progression metastasis. Among various pathways, EGFR, ER, Notch, Hedgehog pathways have recently been identified as in terms proliferation, survival, differentiation, maintenance CSCs, failure. These mediate such MAPK, including MEK/ERK that promote common pro-oncogenic signaling, whereas dysregulation PI3K/Akt, Wnt/β-catenin, JAK/STAT activates key oncogenic events drug resistance, CSC enrichment, metabolic reprogramming. Additionally, these orchestrate an intricate interplay between stromal cells, immune cells. Metabolic reprogramming adaptations contribute to aggressive are unresponsive therapy. Herein, recent insights into novel operating TME aid advancement emphasized current developments practices targeting enhance treatment efficacy reviewed.

Language: Английский

Citations

1

Melatonin: A Potential Regulator of DNA Methylation DOI Creative Commons
Kinga Linowiecka, Andrzej Słomiński, Russel J. Reıter

et al.

Antioxidants, Journal Year: 2023, Volume and Issue: 12(6), P. 1155 - 1155

Published: May 25, 2023

The pineal gland-derived indoleamine hormone, melatonin, regulates multiple cellular processes, ranging from chronobiology, proliferation, apoptosis, and oxidative damage to pigmentation, immune regulation, mitochondrial metabolism. While melatonin is best known as a master regulator of the circadian rhythm, previous studies also have revealed connections between cycle disruption genomic instability, including epigenetic changes in pattern DNA methylation. For example, secretion associated with differential gene methylation night shift workers regulation during embryonic development, there accumulating evidence that can modify Since latter one impacts cancer initiation, also, non-malignant diseases targeting has become novel intervention target clinical therapy, this review discusses potential role an under-investigated candidate regulator, namely by modulating via mRNA protein expression methyltransferases (DNMTs) ten-eleven translocation (TET) proteins. Furthermore, since may impact pattern, authors suggest its possible use combination therapy drugs new anticancer strategy.

Language: Английский

Citations

21

Omics Technologies Improving Breast Cancer Research and Diagnostics DOI Open Access

Arianna Orsini,

Chiara Diquigiovanni, Elena Bonora

et al.

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(16), P. 12690 - 12690

Published: Aug. 11, 2023

Breast cancer (BC) has yielded approximately 2.26 million new cases and caused nearly 685,000 deaths worldwide in the last two years, making it most common diagnosed type world. BC is an intricate ecosystem formed by both tumor microenvironment malignant cells, its heterogeneity impacts response to treatment. Biomedical research entered era of massive omics data thanks high-throughput sequencing revolution, quick progress widespread adoption. These technologies—liquid biopsy, transcriptomics, epigenomics, proteomics, metabolomics, pharmaco-omics artificial intelligence imaging—could help researchers clinicians better understand formation evolution BC. This review focuses on findings recent multi-omics-based that been applied research, with introduction every technique their applications for different phenotypes, biomarkers, target therapies, diagnosis, treatment prognosis, provide a comprehensive overview possibilities research.

Language: Английский

Citations

19

Epigenetic Therapies in Triple-Negative Breast Cancer: Concepts, Visions, and Challenges DOI Open Access
Ulrich Lehmann

Cancers, Journal Year: 2024, Volume and Issue: 16(12), P. 2164 - 2164

Published: June 7, 2024

Breast cancer, the most frequent malignancy in women worldwide, is a molecularly and clinically very heterogeneous disease. Triple-negative breast cancer defined by absence of hormone receptor growth factor ERBB2/HER2 expression. It characterized more aggressive course disease shortage effective therapeutic approaches. Hallmarks cells are not only genetic alterations, but also epigenetic aberrations. The studied best understood alterations methylation DNA base cytosine covalent modification histone proteins. reversibility these modifications make them attractive targets for intervention, as documented numerous ongoing clinical trials. Epidrugs, targeting modifications, might offer new options treating triple-negative cancer. Currently, promising combination therapies which epidrug increases efficiency immuncheckpoint inhibitors. This review focusses exclusively on modifications. In reviewing knowledge about especially focus explaining concepts raising awareness what yet known has to be clarified future.

Language: Английский

Citations

6

Estrogen receptors and extracellular matrix: the critical interplay in cancer development and progression DOI Creative Commons

Sylvia Mangani,

Zoi Piperigkou,

Nikolaos E. Koletsis

et al.

FEBS Journal, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 16, 2024

Cancer remains a significant global health concern. Breast cancer is multifaceted and prevalent disease influenced by several factors, among which estrogen receptors (ERs) the extracellular matrix (ECM) play pivotal roles. ERs, encompassing ERα ERβ, exert diversity on tumor behavior, cell signaling, invasion, metastatic potential, thus guiding breast prognosis. Understanding multifunctional connections between ERs ECM that mediate dynamics of microenvironment vital for unraveling complexity pathobiology identifying novel therapeutic targets. This critical review delves into intricate nature emphasizing their structural isoforms consequential impact outcomes. A detailed examination ER‐mediated signaling pathways reveals how differential expression ERβ influence behavior. The functional ERs‐matrix interactions emerge as factor in modulating epigenetic mechanisms cells, orchestrating changes cellular phenotype patterns modulators. Specifically, are shown to regulate cascades, while effects components activity highlight bidirectional regulatory axis. also highlighted, illustrating distinct contribution ECM‐mediated responses. underscores complex interplay ERα/β ECM, shedding light onto potential strategies targeting these improve management.

Language: Английский

Citations

6

Epigenetic Modulations in Breast Cancer: An Emerging Paradigm in Therapeutic Implications DOI Creative Commons
Shilpi Sarkar,

Dheepika Venkatesh,

Thirukumaran Kandasamy

et al.

Frontiers in Bioscience-Landmark, Journal Year: 2024, Volume and Issue: 29(8)

Published: Aug. 19, 2024

Breast cancer, a heterogeneous and intricate disease, ranks among the leading causes of mortality in women. Restricted therapeutic choices, drug resistance, recurrence, metastasis are predominant conditions that lead to mortality. Accumulating evidence has shown breast cancer initiation progression happen through multifaceted process involves numerous genetic epigenetic alterations. The modulation gene expression modifications, encompassing DNA methylation, histone alterations, non-coding RNA regulation, emerged as fascinating field represents new avenue for therapy. This review emphasizes various aberrant regulations implicated onset advancement cancer. critical modifications closely associated with estrogen signaling, epithelial-to-mesenchymal transition (EMT), stemness, resistance have been discussed extensively. Moreover, it highlights current epi-drugs, including modifying agents, acetyltransferase inhibitors, deacetylase methyltransferase demethyltransferase inhibitors used treatment. Nonetheless, we described investigations pertaining combination therapy employing epi-drugs future challenges.

Language: Английский

Citations

4

Latest Therapeutical Approaches for Triple-Negative Breast Cancer: From Preclinical to Clinical Research DOI Open Access
Mariona Pont, Marta Marqués, Anabel Sorolla

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(24), P. 13518 - 13518

Published: Dec. 17, 2024

Triple-negative breast cancer (TNBC) represents roughly one-sixth of all patients, but accounts for 30–40% deaths. Due to the lack typical biomarkers exploited clinically cancer, it remains very difficult treat. Moreover, its intrinsic high heterogeneity and proneness become resistant drugs administered makes treatment management challenging oncologists. Herein, we outline different therapies used currently TNBC list ongoing clinical trials provide an overview most recent therapeutic landscape. In addition, highlight emerging in preclinical stage that hold promise, such as epigenetic modulators, CRISPR, miniproteins, radioconjugates, vaccines, PROTACs. navigate through existing limitations challenges which hamper development new more effective treatments TNBC. Lastly, point directions may revolutionize future therapy

Language: Английский

Citations

4

Evaluation of the Histone Deacetylase 2 (HDAC-2) Expression in Human Breast Cancer DOI Open Access
Christos Damaskos, Iason Psilopatis, Anna Garmpi

et al.

Cancers, Journal Year: 2024, Volume and Issue: 16(1), P. 209 - 209

Published: Jan. 1, 2024

Background/Aim: Triple negative breast cancer belongs to the most aggressive forms. Histone deacetylases (HDACs) constitute a class of enzymes that exhibit significant role in genesis and progression. In this study, we aimed at assessing clinical importance HDAC-2 triple cancer. Materials Methods: A total 138 specimens were examined on an immunohistochemical basis. statistical analysis was performed order examine association between survival clinicopathological features patients. Results: Increased expression observed every fourth case with positive staining, whereas only 12 out 98 non-triple samples showed high expression. overexpression correlated prolonged overall (OS) disease-free (DFS) Conclusions: High levels seem positively influence patient survival, disease stage recurrence.

Language: Английский

Citations

3

Cellular Epigenetic Targets and Epidrugs in Breast Cancer Therapy: Mechanisms, Challenges, and Future Perspectives DOI Creative Commons

Ibrahim S. Alalhareth,

Saleh M. Alyami,

Abdulrhman Alshareef

et al.

Pharmaceuticals, Journal Year: 2025, Volume and Issue: 18(2), P. 207 - 207

Published: Feb. 3, 2025

Breast cancer is the most common malignancy affecting women, manifesting as a heterogeneous disease with diverse molecular characteristics and clinical presentations. Recent studies have elucidated role of epigenetic modifications in pathogenesis breast cancer, including drug resistance efflux characteristics, offering potential new diagnostic prognostic markers, treatment efficacy predictors, therapeutic agents. Key include DNA cytosine methylation covalent modification histone proteins. Unlike genetic mutations, reprogramming landscape epigenome promising targeted therapy for reversal resistance. Epidrugs, which target modifications, can provide novel options by reversing acquired to treatment. Currently, approach involves combination therapies consisting epidrugs immune checkpoint inhibitors. This review examines aberrant regulation initiation progression, focusing on related estrogen signaling, resistance, epithelial–mesenchymal transition (EMT). It existing drugs treating agents that modify DNA, inhibitors acetyltransferases, deacetylases, methyltransferases, demethyltransferases. also delves into ongoing combining other addresses upcoming obstacles this field.

Language: Английский

Citations

0