Scope of this article
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Editorial general information — not a clinical-review record
Published: Updated: Publisher: Dr. Murat Toktamışoğlu
Extracellular vesicles carry intercellular signals and are studied both in cancer mechanisms and as research tools. That does not prove a commercial skin product causes cancer, but a claim of complete safety in active or prior cancer is not justified without product-specific long-term human data.
This translation has no recorded clinical or medical-language review.
EVs released by tumours and surrounding cells are studied in immunity, angiogenesis, drug resistance and cell communication. EVs are also investigated as delivery and treatment platforms. These different contexts cannot be reduced to 'exosomes cause cancer' or 'exosomes prevent cancer'. A mechanism cannot be inferred for a commercial mixture without knowing its cell source, cargo and manufacturing.
EV-based clinical studies span different diseases, sources, manufacturing processes, doses and routes. Large comparative long-term safety data for aesthetic facial use remain limited. A rare or delayed event may not appear in a small study. The absence of living cells does not mean a product is biologically inactive or carries the same uncertainty for every person.
Coordinate with oncology and the relevant specialist when there is active cancer, recent treatment, immune suppression, an unexplained growing lesion or recurrence surveillance. An elective procedure must not delay diagnosis or treatment or obscure a lesion being followed. Offer deferral when product-specific evidence and official status cannot be shown, and avoid a general promise of safety.
This content is not diagnosis, prescribing, personal risk assessment or a treatment plan. Sources may be limited to a particular product, device, task, indication or study group.
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Foppiani JA et al. · 2025
Scope and limitations: Interpret this source only within the exact product, device, method, indication and study population it names. It does not establish personal suitability, Turkish authorization, a universal protocol or a guaranteed outcome; consult the full source and current local information.
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Austin GK, Struble SL, Quatela VC · 2022
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Sanyal RD, Fabi SG · 2024
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U.S. Food and Drug Administration (FDA) · 2025
Scope and limitations: Interpret this source only within the exact product, device, method, indication and study population it names. It does not establish personal suitability, Turkish authorization, a universal protocol or a guaranteed outcome; consult the full source and current local information.
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Pour Mohammad A et al. · 2023
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Mirza HN, Mirza FN, Khatri KA · 2021
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U.S. Food and Drug Administration (FDA) · 2023
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Systematic review authors · 2024
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International Society for Extracellular Vesicles consensus authors · 2024
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U.S. Food and Drug Administration (FDA) · 2019
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Editorial source — not a signed clinical review