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Elucidating Role of Reactive Oxygen Species (ROS) in Cisplatin Chemotherapy: A Focus on Molecular Pathways and Possible Therapeutic Strategies.

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TLDR
Wang et al. as mentioned in this paper discussed the association of ROS with Cisplatin sensitivity/resistance, and in particular, how molecular pathways, both upstream and downstream targets, can affect the response of cancer cells to CP chemotherapy, and anti-tumor compounds such as curcumin, emodin, chloroquine that regulate ROS and related molecular pathways in increasing CP sensitivity are described.
Abstract
The failure of chemotherapy is a major challenge nowadays, and in order to ensure effective treatment of cancer patients, it is of great importance to reveal the molecular pathways and mechanisms involved in chemoresistance. Cisplatin (CP) is a platinum-containing drug with anti-tumor activity against different cancers in both pre-clinical and clinical studies. However, drug resistance has restricted its potential in the treatment of cancer patients. CP can promote levels of free radicals, particularly reactive oxygen species (ROS) to induce cell death. Due to the double-edged sword role of ROS in cancer as a pro-survival or pro-death mechanism, ROS can result in CP resistance. In the present review, association of ROS with CP sensitivity/resistance is discussed, and in particular, how molecular pathways, both upstream and downstream targets, can affect the response of cancer cells to CP chemotherapy. Furthermore, anti-tumor compounds, such as curcumin, emodin, chloroquine that regulate ROS and related molecular pathways in increasing CP sensitivity are described. Nanoparticles can provide co-delivery of CP with anti-tumor agents and by mediating photodynamic therapy, and induce ROS overgeneration to trigger CP sensitivity. Genetic tools, such as small interfering RNA (siRNA) can down-regulate molecular pathways such as HIF-1α and Nrf2 to promote ROS levels, leading to CP sensitivity. Considering the relationship between ROS and CP chemotherapy, and translating these findings to clinic can pave the way for effective treatment of cancer patients.

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Wnt/β-Catenin Signaling as a Driver of Hepatocellular Carcinoma Progression: An Emphasis on Molecular Pathways.

TL;DR: In this article, the role of Wnt signaling in hepatocellular carcinoma (HCC) and its association with progression and therapy response based on pre-clinical and clinical evidence is discussed.
References
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Journal ArticleDOI

An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress

TL;DR: A signaling pathway initiated by eIF2alpha phosphorylation protects cells against metabolic consequences of ER oxidation by promoting the linked processes of amino acid sufficiency and resistance to oxidative stress.
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Inhibition of Cell Division in Escherichia coli by Electrolysis Products from a Platinum Electrode

TL;DR: In E. coli, the presence of certain group VIIIb transition metal compounds in concentrations of about 1–10 parts per million of the metal in the culture medium causes an inhibition of the cell division process, which implies that the growth process is not markedly affected.
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Reactive oxygen species (ROS) as pleiotropic physiological signalling agents.

TL;DR: This work focuses on ROS at physiological levels and their central role in redox signalling via different post-translational modifications, denoted as ‘oxidative eustress’.
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Coping with stress: eIF2 kinases and translational control

TL;DR: While many of the genes induced by eIF2 phosphorylation are shared between different environmental stresses, eIF1 kinases function in conjunction with other stress-response pathways, such as those regulated by mitogen-activated protein kinases, to elicit gene expression programmes that are tailored for the specific stress condition.
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Mitotic Phosphorylation of Dynamin-related GTPase Drp1 Participates in Mitochondrial Fission

TL;DR: Results suggest that phosphorylation of Drp1 on Ser-585 promotes mitochondrial fission in mitotic cells, and exogenous expression of unphosphorylated mutantDrp1S585A led to reduced mitotic mitochondrial fragmentation.
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