Recent research is highlighting a connection between the SARS-CoV-2 spike protein, DNA damage and an increased risk of developing cancer.

In the first week of October a Swedish research team published a study revealing the spike protein can enter the nucleus of a person’s cells.

For those of you who may be unaware of what the nucleus does, it houses the majority of our genetic material and is the primary control center, or brain, of the cell. It is a sacred place where spike proteins should not be able to gain access.

The researchers also found that once the spike protein enters the nucleus it inhibits proper repair of damaged DNA, specifically Double-Stranded Breaks {DSB}.

Spike Proteins May Damage DNA, Increasing Cancer Risk

Double-Stranded DNA Break {DSB}

DSBs are the most significant class of DNA damage. If DSBs are repaired incorrectly, too slowly, or fail to be repaired whatsoever, this could result in massive loss of genetic information, cell death, or the early steps of cancer cell formation.

The study explains, “Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site… 

Why is this such a huge discovery?

At the beginning of the Covid-19 vaccine rollout we were told, repeatedly, that the spike protein cannot enter the nucleus or alter DNA. However, this study appears to fly in the face of statements like those:

“Our findings reveal a potential molecular mechanism by which the spike protein might impede adaptive immunity and underscore the potential side effects of full-length spike-based vaccines… NHEJ repair and homologous recombination (HR) repair are two major DNA repair pathways that not only continuously monitor and ensure genome integrity but are also vital for adaptive immune cell functions.”

Let’s break this down a little bit.

In normal, replicating cells, the NHEJ genetic pathway repairs 75% of double-stranded DNA breaks while the HR genetic pathway repairs the remaining 25%. Together, the two pathways handle 100% of DSB repair throughout cellular DNA.

For the in vitro {meaning: outside the living body} study, scientists created various treatments intended to cause DNA damage and then examined the NHEJ and HR repair pathways at work. They found that in the presence of the spike proteins, DSB repair decreased by almost 80%.

The study states, “To determine how the spike protein inhibits both NHEJ and HR repair pathways, we analyzed the recruitment of BRCA1 and 53BP1, which are the key checkpoint proteins for HR and NHEJ repair, respectively. We found that the spike protein markedly inhibited both BRCA1 and 53BP1 foci formation…”

BRCA1 and 53BP1 are the key checkpoint proteins for NHEJ and HR repair, and BOTH of these checkpoints were inhibited by spike.

The acronyms BRCA and 53BP1 should seem familiar to many people, as these are well-known within the cancer industry.

Women who inherit mutations in the BRCA1 or BRCA2 pathway have a much higher risk of developing breast cancer throughout their lifetime. Nearly 40-50% higher.

53BP1 is referred to as “The Guardian of the Genome” and is a key player in preventing and mitigating cancer. Any loss of function or abnormal expression of 53BP1 can contribute to tumor occurrence and development, and can drive progression or metastasis in present tumor tissues.

This is significant, given that the vaccine inserts show that the vaccines were NOT evaluated for cancer risk.

In Comirnaty’s prescribing information on the FDA’s website, section 13.1, it states “COMIRNATY has not been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility.”

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

Source: The Highwire Episode 241 “Sins of Silence”

Comirnaty, which is the only vaccine to have been given the green light to enter the FDA approval process, isn’t even available in the United States. If this hasn’t been evaluated for carcinogenicity, imagine what the EUA-only vaccines have or haven’t been evaluated-for?

This revelatory information should not be taken lightly, either by laypersons or the scientific community. It should be re-investigated and reconfirmed through multiple other research studies.

If, through repeated validation, this discovery turns out to be true, it could spell a complete disaster in the coming years for those who’ve been injected with such mRNA technology.


  1. The Highwire, Episode 241: Sins Of Science, “Is Spike Protein Causing Catastrophic Damage to DNA?”
  2. “SARS–CoV–2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro”,
  3. “53BP1: A key player of DNA damage response with critical functions in cancer”,
  4. FDA Highlights of Prescribing Information,
  5. “Comparison of non-homologous end joining and homologous recombination in human cells”,
  6. “Spike protein inside nucleus enhancing DNA damage? – COVID-19 mRNA vaccines update 18”,

References for Genetics & Cancer

  1. “Are There Specific Gene Defects Involved in Breast Cancer?”
  2. “Interview On The Breast Cancer Conqueror Podcast with Dr. V”
  3. “SNP Defects and Cancer”
  4. “Cancer Genes – The Book”

References for Spike Protein Detoxification:

  1. “Confused About Vaxxx Reactxxx? Watch this”
  2. “Targeted Protocols to Help Detox from Vaccines”