TY - JOUR
T1 - Time-Series Analysis of Tumorigenesis in a Murine Skin Carcinogenesis Model
AU - Aoto, Yoshimasa
AU - Okumura, Kazuhiro
AU - Hachiya, Tsuyoshi
AU - Hase, Sumitaka
AU - Wakabayashi, Yuichi
AU - Ishikawa, Fuyuki
AU - Sakakibara, Yasubumi
N1 - Funding Information:
This work was supported by Grant-in-Aid for KAKENHI (Grant-in-Aid for Scientific Research) on Scientific Research (A) No. 23241066 and Scientific Research (S) No. 22220012 from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and JSPS KAKENHI Grant Number 16H06279, and MEXT-Supported Program for the Strategic Research Foundation at Private Universities, 2014–2018. We thank the bioinformatics laboratory members of Keio University, especially Dr. Kengo Sato and Ms. Aki Ohama. Dr. Kengo Sato provided fruitful comments and Ms. Aki Ohama assisted with the Illumina sequencing.
Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Recent years have witnessed substantial progress in understanding tumor heterogeneity and the process of tumor progression; however, the entire process of the transition of tumors from a benign to metastatic state remains poorly understood. In the present study, we performed a prospective cancer genome-sequencing analysis by employing an experimental carcinogenesis mouse model of squamous cell carcinoma to systematically understand the evolutionary process of tumors. We surgically collected a part of a lesion of each tumor and followed the progression of these tumors in vivo over time. Comparative time-series analysis of the genomes of tumors with different fates, i.e., those that eventually metastasized and regressed, suggested that these tumors acquired and inherited different mutations. These findings suggest that despite the occurrence of an intra-tumor selection event for malignant alteration during the transformation from early- to late-stage papilloma, the fate determination of tumors might be determined at an even earlier stage.
AB - Recent years have witnessed substantial progress in understanding tumor heterogeneity and the process of tumor progression; however, the entire process of the transition of tumors from a benign to metastatic state remains poorly understood. In the present study, we performed a prospective cancer genome-sequencing analysis by employing an experimental carcinogenesis mouse model of squamous cell carcinoma to systematically understand the evolutionary process of tumors. We surgically collected a part of a lesion of each tumor and followed the progression of these tumors in vivo over time. Comparative time-series analysis of the genomes of tumors with different fates, i.e., those that eventually metastasized and regressed, suggested that these tumors acquired and inherited different mutations. These findings suggest that despite the occurrence of an intra-tumor selection event for malignant alteration during the transformation from early- to late-stage papilloma, the fate determination of tumors might be determined at an even earlier stage.
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U2 - 10.1038/s41598-018-31349-x
DO - 10.1038/s41598-018-31349-x
M3 - Article
C2 - 30158594
AN - SCOPUS:85052714554
SN - 2045-2322
VL - 8
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 12994
ER -