Pllans-II Induces Cell Death in Cervical Cancer Squamous Epithelial Cells via Unfolded Protein Accumulation and Endoplasmic Reticulum Stress.
Alejandro Montoya-GómezNelson Rivera FrancoLeonel Ives Montealegre-SanchezLuis Manuel Solano-RedondoAndrés CastilloMildrey Mosquera-EscuderoEliécer Jiménez-CharrisPublished in: Molecules (Basel, Switzerland) (2022)
Due to the lack of chemotherapeutic drugs that selectively affect cervical cancer cells, natural sources such as snake venom are currently being investigated for molecules with antitumor potential. Pllans-II , a phospholipase A 2 type-Asp49 from Porthidium lansbergii lansbergii snake venom, induced cell death in a cervical cancer cell line-Ca Ski-related to dysfunction in the ability to resolve endoplasmic reticulum stress, evidenced by sub-expression of genes such as PERK, ERO1 PDIs, HSP70, and CHOP. Western blot analysis validated the last two genes' sub-expression at the protein level. In addition, Pllans-II presented a dose-dependent cytotoxic effect on cancer cells and an insignificant effect on healthy endothelial cells (HUVEC). Additionally, Pllans-II inhibited cancer cells' adhesion and migration capacity, induced cell cycle arrest in the G2/M phase, and induced apoptosis stimulated possibly by the extrinsic route. These results demonstrate for the first time that Pllans-II has an antitumor effect on a squamous epithelial cervical cancer cell line and represents a possible biotechnological tool for designing a prominent antitumor agent.
Keyphrases
- endoplasmic reticulum stress
- induced apoptosis
- cell death
- cell cycle arrest
- endothelial cells
- high glucose
- oxidative stress
- poor prognosis
- binding protein
- low grade
- high grade
- signaling pathway
- diabetic rats
- escherichia coli
- diffuse large b cell lymphoma
- long non coding rna
- amino acid
- biofilm formation
- climate change
- genome wide identification
- cell proliferation
- dna methylation
- candida albicans
- heat stress
- atomic force microscopy