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Watanabe-Asano, T., Kuma, A. and Mizushima, N. (2014) Cycloheximide Inhibits Starvation-Induced Autophagy through mTorc1 Activation. Biochemical and Biophysical Research Communications, 445, 334-339.
https://doi.org/10.1016/j.bbrc.2014.01.180

has been cited by the following article:

• TITLE: Contributors to Cancer Susceptibility, Development and Treatment: Cyclic Nucleotides, Steroids and Autophagy Modulators

  AUTHORS: Wynford Robert Williams

  KEYWORDS: Apoptosis, Chemotherapy, Molecular Similarity, Breast Cancer, Prostate Cancer

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.10 No.2, February 14, 2022

  ABSTRACT: Cell autophagy and apoptosis processes are of interest in drug development and contribute to the chemotherapy outcomes of patients receiving cancer treatment. The functional roles of cyclic nucleotides in cells include maintenance of metabolic homeostasis. cGMP and steroid compounds participate in apoptotic and autophagic events, and modulate the function of multi-drug resistance proteins. Endogenous steroid and cyclic nucleotide ratios change with ageing and this may initiate detrimental changes in cell function. This study uses a computational chemistry approach to investigate molecular similarity within chemotherapeutic and steroid compound structures. Modulators of autophagy/apoptosis and endogenous steroid structures all demonstrate molecular similarity to the structure of cGMP. Relative molecular similarity within these structures facilitates additive and synergistic treatment effects. Endogenous steroids are natural modulators of autophagy and apoptosis; concentration changes consequently have the potential to impact cancer risks.