Publications by authors named "M Constanza Maldifassi"

Background And Purpose: ATP is highly accumulated in secretory vesicles and secreted upon exocytosis from neurons and endocrine cells. In adrenal chromaffin granules, intraluminal ATP reaches concentrations over 100 mM. However, how these large amounts of ATP contribute to exocytosis has not been investigated.

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Article Synopsis
  • While P2X7 receptors (P2X7R) on tumor cells support cancer growth and spread, their expression in the immune system is crucial for initiating immune responses against tumors.
  • Research shows mixed roles of P2X7R in immune regulation, leading to a scarcity of effective P2X7R-targeting drugs in clinical trials.
  • The review explores the prognostic implications of P2X7R, techniques for targeting it in tumor models, and strategies to counter tumor-induced immune evasion through P2X7R to improve cancer immunotherapy.
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Although 2D in vitro cancer cell cultures have been used for decades as a first line-of-research tool to investigate antitumoral drugs and treatments, their use presents many drawbacks, including the poor resemblance of such cultures to the characteristics of in vivo tumors. To mitigate these drawbacks, 3D culture models have emerged as a more representative alternative. Cancer cells cultured as 3D structures have the advantage of resembling solid tumors in their architecture and in their resistance to chemotherapeutic drugs, in part because of restrained drug penetration.

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Nicotine in tobacco is known to induce tumor-promoting effects and cause chemotherapy resistance through the activation of nicotinic acetylcholine receptors (nAChRs). Many studies have associated the α5 nicotinic receptor subunit (α5), and a specific polymorphism in this subunit, with (i) nicotine administration, (ii) nicotine dependence, and (iii) lung cancer. The α5 gene mRNA is upregulated in several types of cancer, including lung, prostate, colorectal, and stomach cancer, and cancer severity is correlated with smoking.

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Study of 64 nicotinic acetylcholine receptors (nAChRs) as a pharmacological target has recently gained interest because of their involvement in analgesia, control of catecholamine secretion, dopaminergic pathways, and aversive pathways. However, an extensive characterization of the human 64 nAChRs has been vitiated by technical difficulties resulting in poor receptor expression. In 2020, Knowland and collaborators identified BARP (-anchoring and regulatory protein), a previously known voltage-gated calcium channel suppressor, as a novel human 64 chaperone.

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