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Human Blood Serum Counteracts EGFR/HER2-Targeted Drug Lapatinib Impact on Squamous Carcinoma SK-BR-3 Cell Growth and Gene Expression.
Shaban, Nina; Raevskiy, Mikhail; Zakharova, Galina; Shipunova, Victoria; Deyev, Sergey; Suntsova, Maria; Sorokin, Maksim; Buzdin, Anton; Kamashev, Dmitri.
Affiliation
  • Shaban N; Moscow Institute of Physics and Technology, Dolgoprudny, 141701, Russia. shaban.na@phystech.edu.
  • Raevskiy M; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, 117997, Russia.
  • Zakharova G; The National Medical Research Center for Endocrinology, Moscow, 117036, Russia.
  • Shipunova V; World-Class Research Center "Digital Biodesign and Personalized Healthcare", Sechenov First Moscow State Medical University, Moscow, 119991, Russia. raevsky@oncobox.com.
  • Deyev S; World-Class Research Center "Digital Biodesign and Personalized Healthcare", Sechenov First Moscow State Medical University, Moscow, 119991, Russia. galina.s.zakharova@gmail.com.
  • Suntsova M; Moscow Institute of Physics and Technology, Dolgoprudny, 141701, Russia. vika_shipunova@mail.ru.
  • Sorokin M; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, 117997, Russia.
  • Buzdin A; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, 117997, Russia. deyev@ibch.ru.
  • Kamashev D; "Biomarker" Research Laboratory, Institute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, 420008, Russia.
Biochemistry (Mosc) ; 89(3): 487-506, 2024 Mar.
Article de En | MEDLINE | ID: mdl-38648768
ABSTRACT
Lapatinib is a targeted therapeutic inhibiting HER2 and EGFR proteins. It is used for the therapy of HER2-positive breast cancer, although not all the patients respond to it. Using human blood serum samples from 14 female donors (separately taken or combined), we found that human blood serum dramatically abolishes the lapatinib-mediated inhibition of growth of the human breast squamous carcinoma SK-BR-3 cell line. This antagonism between lapatinib and human serum was associated with cancelation of the drug induced G1/S cell cycle transition arrest. RNA sequencing revealed 308 differentially expressed genes in the presence of lapatinib. Remarkably, when combined with lapatinib, human blood serum showed the capacity of restoring both the rate of cell growth, and the expression of 96.1% of the genes expression of which were altered by the lapatinib treatment alone. Co-administration of EGF with lapatinib also restores the cell growth and cancels alteration of expression of 95.8% of the genes specific to lapatinib treatment of SK-BR-3 cells. Differential gene expression analysis also showed that in the presence of human serum or EGF, lapatinib was unable to inhibit the Toll-Like Receptor signaling pathway and alter expression of genes linked to the Gene Ontology term of Focal adhesion.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Récepteur ErbB-2 / Prolifération cellulaire / Récepteurs ErbB / Lapatinib Limites: Female / Humans Langue: En Journal: Biochemistry (Mosc) Année: 2024 Type de document: Article Pays d'affiliation: Russie

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Récepteur ErbB-2 / Prolifération cellulaire / Récepteurs ErbB / Lapatinib Limites: Female / Humans Langue: En Journal: Biochemistry (Mosc) Année: 2024 Type de document: Article Pays d'affiliation: Russie