遗传
遺傳
유전
Hereditas
2015年
11期
1086-1094
,共9页
传染性肿瘤%犬类生殖器传染性肿瘤%袋獾面部肿瘤%海螂血液传染性肿瘤%发生%传染%进化
傳染性腫瘤%犬類生殖器傳染性腫瘤%袋獾麵部腫瘤%海螂血液傳染性腫瘤%髮生%傳染%進化
전염성종류%견류생식기전염성종류%대환면부종류%해랑혈액전염성종류%발생%전염%진화
transmissible tumor%CTVT%DFTD%SSCL%tumorigenesis%transmission%evolution
传染性肿瘤是一类以活细胞形式在个体间异体传播的肿瘤。至今已发现并确定4种,即犬类生殖器传染性肿瘤(Canine transmissible venereal tumor, CTVT)、袋獾面部肿瘤(Tasmanian devil facial tumor disease, DFTD)、海螂血液传染性肿瘤(Soft-shell clams leukemia, SSCL)及仓鼠传染性肿瘤(Hamsters reticulum cell sarcoma, HRCS)。过去几十年,在细胞学、组织学、遗传学等方面的研究证明传染性肿瘤是以活细胞进行传播,CTVT是已知的最古老的哺乳动物体细胞系,DFTD来源于施旺细胞,两者均通过下调 MHC基因表达逃避宿主免疫识别,而在SSCL中普遍存在一个转座子多拷贝数变异。近几年来,DFTD和CTVT基因组测序工作相继完成,有助于从全基因组水平研究传染性肿瘤的发生、传染和进化机制。本文总结了传染性肿瘤的研究进展,并展望了未来10年内传染性肿瘤的研究热点。
傳染性腫瘤是一類以活細胞形式在箇體間異體傳播的腫瘤。至今已髮現併確定4種,即犬類生殖器傳染性腫瘤(Canine transmissible venereal tumor, CTVT)、袋獾麵部腫瘤(Tasmanian devil facial tumor disease, DFTD)、海螂血液傳染性腫瘤(Soft-shell clams leukemia, SSCL)及倉鼠傳染性腫瘤(Hamsters reticulum cell sarcoma, HRCS)。過去幾十年,在細胞學、組織學、遺傳學等方麵的研究證明傳染性腫瘤是以活細胞進行傳播,CTVT是已知的最古老的哺乳動物體細胞繫,DFTD來源于施旺細胞,兩者均通過下調 MHC基因錶達逃避宿主免疫識彆,而在SSCL中普遍存在一箇轉座子多拷貝數變異。近幾年來,DFTD和CTVT基因組測序工作相繼完成,有助于從全基因組水平研究傳染性腫瘤的髮生、傳染和進化機製。本文總結瞭傳染性腫瘤的研究進展,併展望瞭未來10年內傳染性腫瘤的研究熱點。
전염성종류시일류이활세포형식재개체간이체전파적종류。지금이발현병학정4충,즉견류생식기전염성종류(Canine transmissible venereal tumor, CTVT)、대환면부종류(Tasmanian devil facial tumor disease, DFTD)、해랑혈액전염성종류(Soft-shell clams leukemia, SSCL)급창서전염성종류(Hamsters reticulum cell sarcoma, HRCS)。과거궤십년,재세포학、조직학、유전학등방면적연구증명전염성종류시이활세포진행전파,CTVT시이지적최고로적포유동물체세포계,DFTD래원우시왕세포,량자균통과하조 MHC기인표체도피숙주면역식별,이재SSCL중보편존재일개전좌자다고패수변이。근궤년래,DFTD화CTVT기인조측서공작상계완성,유조우종전기인조수평연구전염성종류적발생、전염화진화궤제。본문총결료전염성종류적연구진전,병전망료미래10년내전염성종류적연구열점。
Transmissible tumors are a class of tumor that can be transmitted between individuals through liv-ing cells. So far, four types of transmissible tumors including canine transmissible venereal tumor (CTVT),Tasmanian devil facial tumor disease (DFTD), soft-shell clams leukemia (SSCL), and hamsters reticulum cell sarcoma (HRCS)have been discovered and identified. In the last decades, these transmissible tumors have been proved to be transmitted through living cells by cytological, histological and genetic studies. CTVT, the oldest mammalian somat-ic cell line, and DFTD originated from Schwann cell have been reported to avoid immunological recognition by down-regulatingMHC expression, while a high copy number of Steamer retrotransposon is commonly exist in SSCL. In recent years, the whole-genome sequencing of CTVT and DFTD have been completed which facilitates studies on the mechanisms of tumorigenesis, transmission and evolution of transmissible tumors at the whole-genome level. In this review, we summarize the recent advances in transmissible tumors and discuss the research focus in next decade.