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Frances E. Knock, PhD, MD; Raymond M. Galt, MD; Y. T. Oester, MD

JAMA. 1967;202(6):550-551.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

To the Editor:—

Sensitivity tests on hundreds of animal and human cancers have shown greater attack on cancers than normal tissues by selected drugs reacting with sulfhydryl (SH) groups, drugs termed SH inhibitors.^1-3 Nature herself appears to control cell division by regulating SH groups.⁴

Cancer probably devolves to derangement of regulatory mechanisms for mitosis about which little is known except that very large numbers of chemical reactions must occur simultaneously or in interrelated sequence for mitosis to occur. Either huge numbers of separate regulatory mechanisms and separate chemical receptors for regulators may be involved, or a single common chemical denominator may be crucial in turning on and off the host of reactions. Because of its inherent simplicity, the latter hypothesis may be the more probable.^3,4

Protein-SH groups play essential roles at multiple levels of cell control processes. To earlier data^1-5 on the importance of protein-SH groups . . . [Full Text PDF of this Article]

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