Editorial: Epigenetic, molecular and programming mechanisms of renal physiology and pathophysiology DOI Creative Commons
Guiomar Nascimento Gomes, Karina Thieme, Syamantak Majumder

и другие.

Frontiers in Physiology, Год журнала: 2023, Номер 14

Опубликована: Фев. 10, 2023

EDITORIAL article Front. Physiol., 10 February 2023Sec. Renal Physiology and Pathophysiology Volume 14 - 2023 | https://doi.org/10.3389/fphys.2023.1158436

Язык: Английский

Ferrostatin-1 improves neurological impairment induced by ischemia/reperfusion injury in the spinal cord through ERK1/2/SP1/GPX4 DOI

Sidan Liu,

Fengshou Chen, Jie Han

и другие.

Experimental Neurology, Год журнала: 2023, Номер 373, С. 114659 - 114659

Опубликована: Дек. 21, 2023

Язык: Английский

Процитировано

11

Ferroptosis-related signaling pathways in cancer drug resistance DOI Open Access
Yang Yang‐Hartwich,

Simin Yu,

Wanyao Liu

и другие.

Cancer Drug Resistance, Год журнала: 2025, Номер 8(1)

Опубликована: Янв. 6, 2025

Ferroptosis is an iron-dependent form of programmed cell death induced by lipid peroxidation. This process regulated signaling pathways associated with redox balance, iron metabolism, and metabolism. Cancer cells' increased demand makes them especially susceptible to ferroptosis, significantly influencing cancer development, therapeutic response, metastasis. Recent findings indicate that cells can evade ferroptosis downregulating key related this process, contributing drug resistance. underscores the possibility modulating as approach counteract resistance enhance efficacy. review outlines involved in their interactions cancer-related pathways. We also highlight current understanding resistance, offering insights into how targeting provide novel approaches for drug-resistant cancers. Finally, we explore potential ferroptosis-inducing compounds examine challenges opportunities development evolving field.

Язык: Английский

Процитировано

0

Targeting ferroptosis in prostate cancer management: molecular mechanisms, multidisciplinary strategies and translational perspectives DOI Creative Commons
Hao Yang, Xuefeng Zhang,

Zongming Jia

и другие.

Journal of Translational Medicine, Год журнала: 2025, Номер 23(1)

Опубликована: Фев. 7, 2025

Язык: Английский

Процитировано

0

Melatonin protects retinal pigment epithelium cells against ferroptosis in AMD via the PI3K/AKT/MDM2/P53 pathway DOI Creative Commons

Ping Wu,

Long Zhao, Yong Du

и другие.

Frontiers in Pharmacology, Год журнала: 2025, Номер 16

Опубликована: Фев. 27, 2025

Oxidative stress-prompted degeneration of the retinal pigment epithelium (RPE) notably contributes to onset age-related macular (AMD). However, pathways leading RPE deterioration and possible preventative strategies are not yet completely comprehended. Ferroptosis was assayed through evaluation lipid peroxidation (C11-BODIPY MDA), reactive oxygen species (ROS), transmission electron microscopy (TEM), iron content measurement, q-PCR, western blotting, immunofluorescence. To assess structure function in mice, ERG (electroretinography), OCT (optical coherence tomography), H&E (hematoxylin eosin) staining were employed. Network pharmacology methods utilized elucidate potential mechanisms underlying melatonin's protective effects against ferroptosis cells AMD. Genetic engineering techniques applied investigate regulatory relationships among phosphatidylinositol 3-kinase (PI3K), protein kinase-B (AKT), murine double minute-2 (MDM2), 53 (P53), solute carrier family 7 member 11 (SLC7A11). In vitro knockdown experiments MDM2 conducted explore its role within cells. Aβ1-40 can trigger Melatonin inhibit oxidative stress induced by exhibits a effect on Aβ1-40-induced AMD, significantly improving mouse retina layer, facilitating restoration visual function. revealed that targets melatonin AMD closely related ferroptosis, indicated predominant associated with PI3K/AKT/MDM2/P53 signaling pathway. Knocking down specific expression weaken inhibitory ferroptosis. suppress cell death via pathway, thereby preventing decelerating progression

Язык: Английский

Процитировано

0

Mechanisms of ferroptosis and targeted therapeutic approaches in urological malignancies DOI Creative Commons
Wenjie Ma, Xiaotian Jiang, Ruipeng Jia

и другие.

Cell Death Discovery, Год журнала: 2024, Номер 10(1)

Опубликована: Окт. 9, 2024

The prevalence of urological malignancies remains a significant global health concern, particularly given the challenging prognosis for patients in advanced disease stages. Consequently, there is pressing need to explore molecular mechanisms that regulate development discover novel breakthroughs diagnosis and treatment. Ferroptosis, characterized by iron-ion-dependent lipid peroxidation, form programmed cell death (PCD) distinct from apoptosis, autophagy, necrosis. Notably, lipid, iron, glutathione metabolism intricately intracellular ferroptosis, playing essential roles progression various neoplasms drug resistance. In recent years, ferroptosis has been found be closely related malignancies. This paper provides an overview involvement pathogenesis malignancies, elucidates governing its regulation, synthesizes diagnosing treating these We aim provide new direction clinical treatment

Язык: Английский

Процитировано

2

Let‐7a‐5p abrogates progression of papillary thyroid carcinoma cells by decreasing nuclear receptor subfamily 6 group a member 1‐mediated lipogenesis DOI
Tao Zhao, Jinghui Sun, Xiangdong Lu

и другие.

Journal of Biochemical and Molecular Toxicology, Год журнала: 2023, Номер 38(1)

Опубликована: Окт. 31, 2023

Abstract Increasing evidence shows that microRNAs (miRNAs) contribute vital roles in papillary thyroid carcinoma (PTC) carcinogenesis, proliferation, invasion, and so on. As the most common endocrine malignancy, there still have largely unknown molecular events. First, our analysis open access database information indicates downregulation of let‐7a‐5p accelerates PTC progression. Next, lentivirus mediates overexpression cells, found suppressed cancer cells proliferation invasion. Interestingly, bioinformatics hints NR6A1 is potential target gene let‐7a‐5p. The regulation was validated by luciferase quantitative reverse transcription polymerase chain reaction (qRT‐PCR) tissue clinic tumors. Moreover, regulated involved lipogensis vitro vivo. Finally, abrogates PCT xenograft tumors growth, expression lipogenesis. Taken together, data suppresses progression through decreased lipogenesis, related let‐7a‐5p/NR6A1axis might be promising candidate targets for treatment.

Язык: Английский

Процитировано

3

Leveraging nuclear receptor mediated transcriptional signaling for drug discovery: Historical insights and current advances DOI

Riya Ben Patel,

Surbhi Kumari Barnwal,

Arabi Mohammed Saleh M A

и другие.

Advances in protein chemistry and structural biology, Год журнала: 2024, Номер unknown, С. 191 - 269

Опубликована: Ноя. 16, 2024

Язык: Английский

Процитировано

0

Editorial: Epigenetic, molecular and programming mechanisms of renal physiology and pathophysiology DOI Creative Commons
Guiomar Nascimento Gomes, Karina Thieme, Syamantak Majumder

и другие.

Frontiers in Physiology, Год журнала: 2023, Номер 14

Опубликована: Фев. 10, 2023

EDITORIAL article Front. Physiol., 10 February 2023Sec. Renal Physiology and Pathophysiology Volume 14 - 2023 | https://doi.org/10.3389/fphys.2023.1158436

Язык: Английский

Процитировано

0