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Beyond CoCl₂: Toward decision-grade hypoxia modeling in gastric cancer histobiology.

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Acta histochemica 2026 Vol.128(2) p. 152333 Sphingolipid Metabolism and Signalin
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PubMed DOI OpenAlex 마지막 보강 2026-04-30
OpenAlex 토픽 · Sphingolipid Metabolism and Signaling Cancer, Hypoxia, and Metabolism ATP Synthase and ATPases Research

Srikanth M, Singh A, Vijayasimha M

📝 환자 설명용 한 줄

Hypoxia is a characteristic, although heterogeneous, of solid tumors, and experimental hypoxia is still far too frequently addressed as a single replaceable phenomenon.

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APA Mulavagili Srikanth, Ajay Singh, M Vijayasimha (2026). Beyond CoCl₂: Toward decision-grade hypoxia modeling in gastric cancer histobiology.. Acta histochemica, 128(2), 152333. https://doi.org/10.1016/j.acthis.2026.152333
MLA Mulavagili Srikanth, et al.. "Beyond CoCl₂: Toward decision-grade hypoxia modeling in gastric cancer histobiology.." Acta histochemica, vol. 128, no. 2, 2026, pp. 152333.
PMID 41931916 ↗

Abstract

Hypoxia is a characteristic, although heterogeneous, of solid tumors, and experimental hypoxia is still far too frequently addressed as a single replaceable phenomenon. Yashiro et al. demonstrate in their recent article in Acta Histochemica that the signaling of lysophosphatidic acid receptor in gastric cancer cells differs significantly in cobalt chloride-induced but not physiological hypoxia with resulting differences in motility and cisplatin response. It is not an observation merely at the receptor level but it reveals a deeper reproducibility and translational issue in tumor biology. Pathway attribution, interpretation of drug-response and prioritization of targets can be misleading when chemical hypoxia is to be used as a surrogate to oxygen deprivation without explicit validation. We believe that this paper must motivate the field-wide to abandon convenience-driven hypoxia modelling in favour of decision-grade hypoxia phenotyping. There should be future work to incorporate physiologically accurate oxygen control, orthogonal confirmation of hypoxic conditions, spatially resolved histochemical reporters and standard reporting of receptor-context interactions. This framework would enhance mechanistic accuracy, enhance cross-study comparability, and expedite translation of hypoxia-informed therapeutic interventions in gastric cancer and other diseases.

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