Differences Between Long- and Short-Term Survivors with Lymphoma Type of Adult T-Cell Leukemia

1990 ◽  
Vol 2 (5) ◽  
pp. 301-305 ◽  
Author(s):  
Yoshinori Shimamot ◽  
Kenji Suga ◽  
Hideya Igarashi ◽  
Junji Nishimura ◽  
Hajime Nawata ◽  
...  
2014 ◽  
Vol 140 (0) ◽  
pp. 74-74
Author(s):  
Hiromi Nagano ◽  
Hiroyuki Iuchi ◽  
Tomohiro Jimura ◽  
Masaki Kawabata ◽  
Yuichi Kurono

Blood ◽  
1986 ◽  
Vol 68 (3) ◽  
pp. 779-782 ◽  
Author(s):  
N Arima ◽  
Y Daitoku ◽  
S Ohgaki ◽  
J Fukumori ◽  
H Tanaka ◽  
...  

Abstract Leukemic cells in the peripheral blood of a patient with adult T cell leukemia (ATL), which expressed the Tac antigen/interleukin 2 (IL2) receptor, were investigated in vitro for autocrine growth by IL 2. The cells showed spontaneous proliferation in mitogen-free medium. The spontaneous proliferation of the cells was inhibited by monoclonal anti- IL 2 or anti-Tac antibody. These cells were found to produce messenger RNA for IL 2 and secrete IL 2 during short-term culture in the same medium. Recombinant IL 2 and IL 2 secreted by the cells enhanced the proliferation of the cells in a dose-dependent manner when added to the initial culture. These findings demonstrate that an autocrine mechanism by IL 2 is involved in the proliferation of ATL cells during short-term culture.


2010 ◽  
Vol 207 (13) ◽  
pp. 2785-2792 ◽  
Author(s):  
Hiba El Hajj ◽  
Marwan El-Sabban ◽  
Hideki Hasegawa ◽  
Ghazi Zaatari ◽  
Julien Ablain ◽  
...  

Chronic HTLV-I (human T cell lymphotropic virus type I) infection may cause adult T cell leukemia/lymphoma (ATL), a disease with dismal long-term prognosis. The HTLV-I transactivator, Tax, initiates ATL in transgenic mice. In this study, we demonstrate that an As2O3 and IFN-α combination, known to trigger Tax proteolysis, cures Tax-driven ATL in mice. Unexpectedly, this combination therapy abrogated initial leukemia engraftment into secondary recipients, whereas the primary tumor bulk still grew in the primary hosts, only to ultimately abate later on. This loss of initial transplantability required proteasome function. A similar regimen recently yielded unprecedented disease control in human ATL. Our demonstration that this drug combination targeting Tax stability abrogates tumor cell immortality but not short-term growth may foretell a favorable long-term efficiency of this regimen in patients.


1990 ◽  
Vol 2 (5) ◽  
pp. 335-340 ◽  
Author(s):  
Yoshinori Shimamoto ◽  
Kenji Suga ◽  
Motoko Shimojo ◽  
Junji Nishimura ◽  
Hajime Nawata ◽  
...  

Cancer ◽  
1989 ◽  
Vol 63 (2) ◽  
pp. 289-294 ◽  
Author(s):  
Yoshinori Shimamoto ◽  
Kazutoshi Ono ◽  
Masayuki Sano ◽  
Miwako Matsuzaki ◽  
Kenji Suga ◽  
...  

1987 ◽  
Vol 49 (5) ◽  
pp. 823-829
Author(s):  
Taizo TAKESHITA ◽  
Hiromaro KIRYU ◽  
Yasushi SAKATA ◽  
Yuichi MIYAMOTO

1995 ◽  
Vol 18 (3-4) ◽  
pp. 317-323 ◽  
Author(s):  
Kimiharu Uozumi ◽  
Shuichi Hanada ◽  
Nobuhito Ohno ◽  
Kenji Ishitsuka ◽  
Shigemi Shimotakahara ◽  
...  

2021 ◽  
Author(s):  
Miku Ishizawa ◽  
Undrakh Ganbaatar ◽  
Atsuhiko Hasegawa ◽  
Natsuko Takatsuka ◽  
Nobuyo Kondo ◽  
...  

2014 ◽  
Vol 107 (6) ◽  
pp. 469-473 ◽  
Author(s):  
Hiromi Nagano ◽  
Hiroyuki Iuchi ◽  
Tomohiro Jimura ◽  
Masaki Kawabata ◽  
Yuichi Kurono

Blood ◽  
2001 ◽  
Vol 98 (4) ◽  
pp. 1160-1165 ◽  
Author(s):  
Nobuhito Ohno ◽  
Ayako Tani ◽  
Kimiharu Uozumi ◽  
Shuichi Hanada ◽  
Tatsuhiko Furukawa ◽  
...  

Chemotherapy of patients with adult T-cell leukemia (ATL) has been unsuccessful. The poor outcome is thought to be caused mainly by the drug resistance of ATL cells. Lung resistance–related protein (LRP) is a novel protein associated with drug resistance. The expression of LRP messenger RNA (mRNA) was evaluated by slot blot analysis in 55 patients with ATL. Of these patients, 36 had acute, 12 chronic, and 7 lymphoma-type ATL. The expression levels of LRP mRNA were significantly higher in chronic ATL than in lymphoma-type ATL (P = .007). The expression of LRP mRNA was higher in patients with white blood cell counts above 30 000/μL (P = .038) or with abnormal lymphocyte counts above 10 000/μL (P = .007) than in the remaining patients. The enhanced efflux of [14C]doxorubicin from nuclei isolated from ATL cells that expressed high levels of LRP was inhibited by a polyclonal antibody against LRP, and the accumulation of doxorubicin in the isolated nuclei was increased by the anti-LRP antibody. In acute and lymphoma-type ATL patients, high expression of LRP mRNA at diagnosis correlated with shorter survival, and a Cox proportional hazards model showed that LRP expression is an independent prognostic factor. These findings suggest that functionally active LRP is expressed in some ATL cells and that it is involved in drug resistance and poor prognosis in ATL.


Sign in / Sign up

Export Citation Format

Share Document