Landmark
study reveals COVID-19 “vaccines” severely disrupt the expression of
thousands of genes—triggering mitochondrial failure, immune
reprogramming, and oncogenic activation.
The study was conducted by scientists from Neo7Bioscience (Dr. John Catanzaro, Dr. Natalia von Ranke, Dr. Wei Zhang, Dr. Philipp Anokin), the University of North Texas (Dr. Danyang Shao, Dr. Ahmad Bereimipour, Minh Vu), theMcCullough Foundation (Dr. Peter McCullough and Nicolas Hulscher) and Medicinal Genomics (Kevin McKernan).
Using high-resolution RNA sequencing of blood samples and differential gene expression analysis, we found that COVID-19
“vaccines” severely disrupted the expression of thousands of
genes—inducing mitochondrial failure, immune system reprogramming, and
oncogenic activation that persisted for months to years after injection.
METHODS
The study analyzed whole blood RNA profiles from:
3 patients with new-onset adverse events (neurological, cardiovascular, chronic fatigue) following mRNA vaccination
7 patients newly diagnosed with cancer post-mRNA vaccination
803 healthy controls
Key tools and analyses:
Bulk RNA sequencing (Illumina NextSeq) of patient blood samples
DESeq2 for differential gene expression analysis
Gene Set Enrichment Analysis (GSEA) to identify disrupted biological pathways
STRING + Cytoscape to visualize protein-protein interaction (PPI) networks of dysregulated genes
FINDINGS
mRNA Vaccines Trigger Transcriptomic Chaos
Both vaccine injured groups showed massive gene dysregulation compared to healthy controls—hundreds of genes up- or down-regulated, especially in pathways tied to:
Mitochondrial dysfunction
Protein folding and degradation stress (proteasome pathways)
Ribosomal overload and nonsense-mediated decay (NMD)
Chronic systemic inflammation
Oncogenic activation (MYC) and tumor suppressor suppression (p53, KRAS)
Shared Hallmarks in Both Groups
Mitochondrial Dysfunction & Oxidative Stress Complex I disruptions and ROS overproduction—core features of chronic fatigue and neurodegeneration.
Ribosomal Stress & Translational Overdrive Synthetic
mRNA with modified bases (N1-methylpseudouridine) appears to trigger
ribosomal overload, translation errors, and RNA surveillance activation.
These stress signatures are also consistent with host responses to
foreign genetic material, and may reflect reverse transcription of mRNA
via endogenous LINE-1 activity, residual plasmid DNA, or vector-derived
promoter activity—raising the possibility of persistent transcription or
genomic integration.
Proteasome Activation Likely due to spike protein persistence and accumulation of misfolded proteins.
Endothelial Dysfunction & Coagulopathy Genes regulating angiogenesis and coagulation were downregulated—mirroring thrombotic complications post-vaccination.
Oncogenic Signals Activation of MYC, suppression of p53 and KRAS inhibitors, setting the stage for tumor growth.
Cancer Group Shows Additional Red Flags
Genomic Instability & Epigenetic Reprogramming Strong
upregulation of genes linked to chromatin remodeling, DNA methylation,
and nucleosome displacement—hallmarks of early tumorigenesis.
Hyperactivation of Type I Interferon and Toll-like Receptor (TLR) Pathways Persistent immune system stimulation via TLRs, IRFs, and JAK-STAT—common in both chronic inflammation and cancer immune escape.
ACE2 Downregulation Both groups showed severe suppression of ACE2, activating the Ang II → AT1R → NF-κB/MAPK cascade—a known tumor-promoting and inflammatory loop.
To
our knowledge, this is the first study to show long-term genetic
disruption in individuals harmed by the COVID-19 mRNA injections.
These findings strongly suggest:
mRNA vaccines can induce gene expression profiles consistent with tumor formation and chronic disease
mRNA-vaccinated individuals may be at heightened risk of cancer, immune dysfunction, and inflammatory disorders
The
synthetic mRNA and long-lasting spike protein appear to create
sustained cellular stress that disrupts normal genetic regulation
Signatures
suggest potential reverse transcription of vaccine mRNA and persistence
of plasmid DNA—raising concern for long-term transcriptional
interference or possible genomic integration
It’s
time for the immediate withdrawal of these dangerous gene therapies to
protect the remaining ~20% of the population still considering booster
doses.
By Independent News Roundup
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