Establishment and characterization of novel cancer cachexia-inducing cell line, Aku60GC, of scirrhous gastric cancer

被引:0
|
作者
Noguchi, Rei [1 ]
Yanagihara, Kazuyoshi [1 ,2 ,3 ]
Iino, Yuki [4 ]
Komatsu, Teruo [4 ]
Kubo, Takanori [2 ]
Ono, Takuya [1 ]
Osaki, Julia [1 ]
Adachi, Yuki [1 ]
Iwata, Shuhei [1 ]
Shiota, Yomogi [1 ]
Seyama, Toshio [2 ]
Kondo, Tadashi [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Rare Canc Res, 5-1-1 Tsukiji,Chuo Ku, Tokyo 1040045, Japan
[2] Yasuda Womens Univ, Fac Pharm, Dept Life Sci, 6-13-1 Yasuhigashi,Asaminami Ku, Hiroshima 7310153, Japan
[3] Biospecimen Labs Inc, 1-5-10-105 Nakamagome,Ohta ku, Tokyo 1430027, Japan
[4] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, 6-5-1 Kashiwanoha, Kashiwa, Chiba 2778577, Japan
关键词
Patient-derived cell line; Cachexia; Whole exome sequence; Cytokine; Scirrhous gastric cancer; STOMACH-CANCER; INTERLEUKIN-18; CARCINOMA; PATHWAY; GROWTH; AKT2;
D O I
10.1007/s13577-025-01208-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cancer cachexia is a pathological state characterized by severe weight loss, skeletal muscle depletion, and adipose tissue reduction. Cancer cachexia is observed in gastric cancer (GC) with a higher incidence over 80%. Approximately 80% patients with advanced GC including scirrhous gastric cancer (SGC), which has the worst prognosis among all GC, are affected with cachexia. The exact pathophysiology in SGC cancer cachexia remains elusive, and therapeutic approaches for the cancer cachexia have not been established. Patient-derived cancer cachexia models are promising for elucidating the underlying mechanisms of disease progression and developing novel treatments, none of which originate from SGC. Therefore, we established a novel cancer cachexia-inducing cell line, designated Aku60GC, through stepwise selection of a patient-derived SGC cell line, HSC-60. Subcutaneous implantation of the Aku60GC cells into nude mice resulted in weight loss, muscle atrophy, and adipose tissue depletion with high reproducibility, accompanied by elevation of the circulating cytokines IL-8 and IL-18. Compared to parental HSC-60 cells, Aku60GC cells exhibited additional genomic changes, such as AKT2 and CCNE1 gains, a somatic mutation of RUNX1, and accelerated growth. Thus, our results demonstrate that the Aku60GC cell line is a valuable resource for research on cancer cachexia in SGC.
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页数:12
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