» Articles » PMID: 34572719

LyeTx I-b Peptide Attenuates Tumor Burden and Metastasis in a Mouse 4T1 Breast Cancer Model

Abstract

Cationic anticancer peptides have exhibited potent anti-proliferative and anti-inflammatory effects in neoplastic illness conditions. LyeTx I-b is a synthetic peptide derived from spider venom that previously showed antibiotic activity in vitro and in vivo. This study focused on the effects of LyeTxI-b on a 4T1 mouse mammary carcinoma model. Mice with a palpable tumor in the left flank were subcutaneously or intratumorally injected with LyeTx I-b (5 mg/kg), which significantly decreased the tumor volume and metastatic nodules. Histological analyses showed a large necrotic area in treated primary tumors compared to the control. LyeTxI-b reduced tumor growth and lung metastasis in the 4T1 mouse mammary carcinoma model with no signs of toxicity in healthy or cancerous mice. The mechanism of action of LyeTx I-b on the 4T1 mouse mammary carcinoma model was evaluated in vitro and is associated with induction of apoptosis and cell proliferation inhibition. Furthermore, LyeTx I-b seems to be an efficient regulator of the 4T1 tumor microenvironment by modulating several cytokines, such as TGF-β, TNF-α, IL-1β, IL-6, and IL-10, in primary tumor and lung, spleen, and brain. LyeTx I-b also plays a role in leukocytes rolling and adhesion into spinal cord microcirculation and in the number of circulating leukocytes. These data suggest a potent antineoplastic efficacy ofLyeTx I-b.

Citing Articles

Encapsulated LyeTx III Peptide: Cytotoxic Agent Isolated from Spider Venom.

Santos D, Santiago L, Santos N, Romao W, Resende J, De Lima M Toxins (Basel). 2025; 17(1).

PMID: 39852985 PMC: 11768708. DOI: 10.3390/toxins17010032.


Screening and validating the optimal panel of housekeeping genes for 4T1 breast carcinoma and metastasis studies in mice.

Souza J, Antunes-Porto A, da Silva Oliveira I, Amorim C, Pires L, de Brito Duval I Sci Rep. 2024; 14(1):26476.

PMID: 39488625 PMC: 11531515. DOI: 10.1038/s41598-024-77126-x.


Venom-derived peptides for breaking through the glass ceiling of drug development.

Freuville L, Matthys C, Quinton L, Gillet J Front Chem. 2024; 12:1465459.

PMID: 39398192 PMC: 11468230. DOI: 10.3389/fchem.2024.1465459.


Investigation of cytotoxic effect and action mechanism of a synthetic peptide derivative of rabbit cathelicidin against MDA-MB-231 breast cancer cell line.

Bashi M, Madanchi H, Yousefi B Sci Rep. 2024; 14(1):13497.

PMID: 38866982 PMC: 11169400. DOI: 10.1038/s41598-024-64400-1.


Cytotoxic, Antibacterial, and Antioxidant Activities of the Leaf Extract of .

Chen P, Lin E, Su H, Huang C Plants (Basel). 2023; 12(4).

PMID: 36840206 PMC: 9967939. DOI: 10.3390/plants12040859.


References
1.
Lau J, Dunn M . Therapeutic peptides: Historical perspectives, current development trends, and future directions. Bioorg Med Chem. 2017; 26(10):2700-2707. DOI: 10.1016/j.bmc.2017.06.052. View

2.
Hutchinson L . Breast cancer: challenges, controversies, breakthroughs. Nat Rev Clin Oncol. 2010; 7(12):669-70. DOI: 10.1038/nrclinonc.2010.192. View

3.
Holm J, Li J, Darabi H, Eklund M, Eriksson M, Humphreys K . Associations of Breast Cancer Risk Prediction Tools With Tumor Characteristics and Metastasis. J Clin Oncol. 2015; 34(3):251-8. DOI: 10.1200/JCO.2015.63.0624. View

4.
Santos D, Verly R, Pilo-Veloso D, De Maria M, de Carvalho M, Cisalpino P . LyeTx I, a potent antimicrobial peptide from the venom of the spider Lycosa erythrognatha. Amino Acids. 2009; 39(1):135-44. DOI: 10.1007/s00726-009-0385-x. View

5.
Iadocicco K, Monteiro L, Chaui-Berlinck J . A theoretical model for estimating the margination constant of leukocytes. BMC Physiol. 2002; 2:3. PMC: 100780. DOI: 10.1186/1472-6793-2-3. View