DMSO inhibits SV40

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An old paper from 1992:
"Repression of SV40 T Oncoprotein Expression by DMSO", by MICHAEL M. WITTE et al. (1992)

(alternative link)

SV40 large T oncoprotein-transformed murine mesenchymal 3T3 T stem cells (CSV3 cells) can be induced to growth arrest and then differentiate into adipocytes. When differentiation occurs, SV40 T oncoprotein expression is repressed (Estervig et al., J Virol 63:2718, 1989).

To determine if repression of T oncoprotein expression can also be induced pharmacologically, the effect of a variety of agents that have been reported to effect differentiation in various cell types but not in 3T3 Tor CSV3 cells was tested. This rationale suggests that if any of these agents repress T oncoprotein expression in CSV3 cells, then the results would establish that repression of T oncoprotein expression can be mediated by mechanisms independent of overt differentiation. The results show that dirnethylsulfoxide (DMSO) is the only agent tested that represses T oncoprotein expression in CSV3 cells. Repression occurs in a dosage-dependent manner within 24-96 hours after exposure to DMSO.

The effect of DMSO on T oncoprotein expression is mediated by posttranslational mechanisms that decrease the stability of the T oncoprotein. DMSO-induced repression of T oncoprotein expression is also associated with reversion of the transformed phenotype in CSV3 cells as demonstrated by the loss of responsiveness to a specific transformation-associated mitogen.
These data support the conclusion that the pharmacological repression of T oncoprotein expression represents a form of cancer suppressor activity that can be mediated by a distinct molecular mechanism.

"Natural News" article:
"DMSO Unmasked: The Natural Cure for Va((ine-Induced Cancer and the SV40 Dep0p[...] Conspiracy" by Mike Adams (01/26/2026)

Introduction: The Hidden Oncoprotein and a Suppressed Remedy

For decades, the specter of a hidden cancer-causing agent has lurked in the syringes of millions, deliberately seeded into what was sold to the public as life-saving immunizations. The contaminant is Simian Virus 40 (SV40), a potent oncogene that was present in the Salk and Sabin polio vaccines administered to countless children and adults across the globe [W-1, W-2].

The question has never been one of accidental oversight, but of deliberate malevolence aimed at depopulation and the ushering in of an age of engineered disease. The Centers for Disease Control and Prevention (CDC) itself has admitted to the historical contamination of polio vaccines with SV40, a virus known to be tumorigenic in laboratory animals and increasingly linked to a wide array of human cancers, including mesotheliomas, brain tumors, and bone cancers [1]. This flips the narrative of safe and effective vaccination on its head, revealing a pattern of contamination that spanned decades and affected millions worldwide.

Simultaneously, an ancient, natural healing molecule has been systematically demonized, restricted, and suppressed by the very institutions entrusted with public health. Dimethyl Sulfoxide (DMSO), a simple, abundant organic sulfur compound derived from trees, has shown a startling ability to repress the expression of the very SV40 T oncoprotein that has been deliberately used as a biological weapon for generations [S-1, S-3, W-3]. This article will expose two intertwined conspiracies: the deliberate lacing of vaccines with cancer-causing SV40 large T oncoproteins as part of a global depopulation agenda, and the systematic, ruthless suppression of DMSO as nature's profound antidote.