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This idea is supported by the observation that bacteria, which lack the HOCl-activated molecular chaperone Hsp33, accumulate a significant number of aggregated proteins and are much more sensitive to HOCl treatment than wild-type cells harboring functional Hsp33 [10]

Importantly, this regulation cascade can be exploited by targeting YBX1 to block AMPK protein synthesis and targeting GLUT1 to induce energy stress, which synergistically blunts tumor growth in vivo

While the intracellular reduction of Cr(VI) to Cr(III), which mostly occurs in the stomach, is believed to be a cause of genotoxicity and carcinogenicity, extracellular reduction is considered to be a detoxifying mechanism

Benitez-Duif PA, Weckes S, Ferreira RMP, Kurka D, Tiller JC

Available at: (Accessed on 14th February 2026)