# Clinical Impact of Semaglutide Beyond Glycemic Control: A Critical Analysis of Oncogenic Potential and Mitigation of Cardiotoxicity

**Authors:** Adriana Correra, Alfredo Mauriello, Valeria Cetoretta, Anna Chiara Maratea, Lucia Riegler, Isabella Di Sarno, Francesco Giallauria, Federico Guerra, Vincenzo Russo, Antonello D’Andrea

PMC · DOI: 10.3390/ph19020297 · Pharmaceuticals · 2026-02-10

## TL;DR

This review examines semaglutide's safety and benefits beyond blood sugar control, focusing on cancer risks and heart protection.

## Contribution

The paper provides a critical analysis of semaglutide's oncogenic potential and cardioprotective effects using recent clinical and epidemiological data.

## Key findings

- Human data do not confirm a significant increase in pancreatic cancer risk with semaglutide use.
- Semaglutide shows cardioprotective properties that may mitigate cardiotoxicity from anticancer therapies.
- Preclinical concerns about thyroid cancer are not supported by human epidemiological evidence.

## Abstract

Introduction: Semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1RA), has demonstrated unprecedented efficacy in the treatment of type 2 diabetes mellitus (T2DM) and obesity. However, its rapid clinical widespread use has ignited a debate regarding long-term safety, particularly concerning the risk of specific neoplasms and its ability to modulate cardiovascular health, not only as primary prevention but also as a potential agent to mitigate cardiotoxicity. Objectives: This narrative review aims to analyze the most recent evidence from clinical trials and post-marketing surveillance to evaluate the correlation between semaglutide use and the incidence of cancer, as well as the drug’s efficacy in reducing cardiotoxicity induced by anticancer therapies. Results and Discussion: While preclinical rodent models suggested a link to medullary thyroid carcinoma, human epidemiological data remain reassuring, though caution is advised in patients with genetic predisposition. Regarding pancreatic cancer, current meta-analyses do not confirm a significant increase in risk, suggesting that metabolic benefits outweigh potential concerns. Conclusions: Semaglutide is confirmed as a therapeutic tool with a highly favorable benefit–risk profile. While oncological monitoring must continue, the drug’s cardioprotective and anti-inflammatory properties open new frontiers not only in metabolic management but also in safeguarding cardiovascular integrity in complex clinical scenarios.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), obesity (MONDO:0011122), medullary thyroid carcinoma (MONDO:0007958), pancreatic cancer (MONDO:0005192)

## Full-text entities

- **Genes:** Itgax (integrin alpha X) [NCBI Gene 16411] {aka Cd11c, Cr4, N418}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, HSPG2 (heparan sulfate proteoglycan 2) [NCBI Gene 3339] {aka HSPG, PLC, PRCAN, SJA, SJS, SJS1}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, RAPGEF3 (Rap guanine nucleotide exchange factor 3) [NCBI Gene 10411] {aka CAMP-GEFI, EPAC, EPAC1, HSU79275, bcm910}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, MMP3 (matrix metallopeptidase 3) [NCBI Gene 4314] {aka CHDS6, MMP-3, SL-1, STMY, STMY1, STR1}, P4HA1 (prolyl 4-hydroxylase subunit alpha 1) [NCBI Gene 5033] {aka P4HA}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, ACSL1 (acyl-CoA synthetase long chain family member 1) [NCBI Gene 2180] {aka ACS1, FACL1, FACL2, LACS, LACS1, LACS2}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, BNIP3 (BCL2 interacting protein 3) [NCBI Gene 664] {aka HABON, NIP3}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562] {aka AMPK, AMPK alpha 1, AMPKa1}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, PAGR1 (PAXIP1 associated glutamate rich protein 1) [NCBI Gene 79447] {aka C16orf53, GAS, PA1}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, CXCR6 (C-X-C motif chemokine receptor 6) [NCBI Gene 10663] {aka BONZO, CD186, CDw186, STRL33, TYMSTR}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}
- **Diseases:** Cancers (MESH:D009369), energetic failure (MESH:D051437), thyroid and pancreatic malignancies (MESH:D010195), digestive tract cancer (MESH:D004067), fibrosis (MESH:D005355), cardiomyocyte injury (MESH:D014947), inflammation (MESH:D007249), mitochondrial damage (MESH:D028361), Pancreatic Cancer (MESH:D010190), KV channel (MESH:C538353), Cardiotoxicity (MESH:D066126), thyroid (MESH:D013966), MTC (MESH:C536914), metabolic disorder (MESH:D008659), Obesity (MESH:D009765), Overweight (MESH:D050177), carcinogenesis (MESH:D063646), myocardial damage (MESH:D009202), papillary thyroid carcinoma (MESH:D000077273), cardiovascular disease (MESH:D002318), hypoglycemia (MESH:D007003), weight loss (MESH:D015431), cytotoxic (MESH:D064420), Thyroid Carcinoma (MESH:D013964), C-cell hyperplasia (MESH:D006965), myocardial necrosis (MESH:D009336), prostate (MESH:D011472), breast cancer (MESH:D001943), T2D (MESH:D003924), gastrointestinal cancers (MESH:D005770)
- **Chemicals:** PIP2 (MESH:D019269), triglycerides (MESH:D014280), oxygen (MESH:D010100), anthracycline (MESH:D018943), cAMP (MESH:D000242), nitric oxide (MESH:D009569), cholesterol (MESH:D002784), GLP-1RA (-), doxorubicin (MESH:D004317), ROS (MESH:D017382), glucose (MESH:D005947), lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Rodentia (rodent, order) [taxon 9989], Cercopithecidae (monkey, family) [taxon 9527]
- **Mutations:** lysine at position 26
- **Cell lines:** 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12943345/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943345/full.md

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Source: https://tomesphere.com/paper/PMC12943345