Intratumoral heterogeneity of c-KIT mutations in a feline splenic mast cell tumor and their functional effects on cell proliferation

• Published in: Scientific reports 2022-09, Vol.12 (1), p.15791-15791, Article 15791
• Main Authors: Hasegawa, Yuki, Shosu, Kazuha, Tsuji, kanako, Shimoyama, Yumiko, Miyama, Takako Shimokawa, Baba, Kenji, Okuda, Masaru, Itamoto, Kazuhito, Igase, Masaya, Mizuno, Takuya
• Format: Article
• Language: English
• Subjects: 631/337; 631/67; 631/67/1059; Amino acid sequence; Amino acids; c-Kit protein; Cell growth; Cell proliferation; Cloning; Exons; Gene deletion; Heterogeneity; Humanities and Social Sciences; Interleukin 3; Kinases; KIT protein; Laboratory tests; multidisciplinary; Mutation; Phosphorylation; Point mutation; Remission; Science; Science (multidisciplinary); Skin; Spleen; Tumor cells; Tumors
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-19089-5

A cat was presented with mast cell tumors (MCTs) of the skin and spleen. During the initial diagnosis, the exon 8 mutation of c-KIT was detected in the masses from skin and spleen by a commercial laboratory test. Consequently, treatment with toceranib was started. After complete remission, because of recurrence on day 117, the spleen and skin tumors were removed, but the cat eventually died on day 191. The analysis of ten cDNA clones of the c-KIT gene cloned from the surgically removed spleen revealed that seven different cDNA patterns were included, indicating the heterogeneity of this gene in the splenic MCT. The seven cDNA nucleotide patterns can be classified into four protein sequence patterns. In addition to the previously known mutations in exon 8, we identified novel mutations in exons 9, 10, and 18; four amino acids deletion in exon 9, and a point mutation in exons 10 and 18. Mouse IL-3-dependent cell line, Ba/F3, was transduced with these mutant clones, and c-KIT phosphorylation and proliferation assays were performed. We found that certain mutations affected the c-KIT phosphorylation status and cell proliferation. This suggests that heterogeneity among the population of tumor cells exists in MCTs, and that the dominant clones of this heterogeneity may contribute to the subsequent tumor cell growth.