Local tumor control and DNA-PK activity of peripheral blood lymphocytes in prostate cancer patients receiving radiotherapy.
Local tumor control and DNA-PK activity of peripheral blood lymphocytes in prostate cancer patients receiving radiotherapy.
复制标题
前列腺癌患者的外周血淋巴细胞的局部肿瘤控制和DNA-PK活性接受放疗。
DOI:
10.1093/jrr/rrw099
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发表时间:
2017-03-01
影响因子:
2
通讯作者:
Sakata KI
中科院分区:
文献类型:
--
作者:
Someya M;Hasegawa T;Hori M;Matsumoto Y;Nakata K;Masumori N;Sakata KI
Repair of DNA damage is critical for genomic stability, and DNA-dependent protein kinase (DNA-PK) has an important role in repairing double-strand breaks. We examined whether the DNA-PK activity of peripheral blood lymphocytes (PBLs) was related to biochemical (prostate-specific antigen: PSA) relapse and radiation toxicity in prostate cancer patients who have received radiotherapy. A total of 69 patients with localized adenocarcinoma of the prostate participated in this study. Peripheral blood was collected 2 years or later after radiotherapy and centrifuged, then DNA-PK activity was measured by a filter binding assay. The high DNA-PK activity group had a significantly higher PSA relapse–free survival rate than the low DNA-PK activity group. The 10-year PSA relapse–free survival was 87.0% in the high DNA-PK activity group, whereas it was 52.7% in the low DNA-PK activity group. Multivariate analysis showed the Gleason score and the level of DNA-PK activity were significant predictors of PSA relapse after radiotherapy. In addition, the low DNA-PK activity group tended to have a higher incidence of Grade 1–2 urinary toxicity than the high DNA-PK activity group. Prostate cancer patients with low DNA-PK activity had a higher rate of PSA relapse and a higher incidence of urinary toxicity. DNA-PK activity in PBLs might be a useful marker for predicting PSA relapse and urinary toxicity, possibly contributing to personalized treatment of prostate cancer.
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DOI:
10.1042/bj20080413
发表时间:
2009-02-01
期刊:
The Biochemical journal
影响因子:
--
作者:
Mahaney BL;Meek K;Lees-Miller SP
通讯作者:
Lees-Miller SP
影响因子:
2
作者:
Yamazaki H;Nakamura S;Nishimura T;Yoshida K;Yoshioka Y;Koizumi M;Ogawa K
通讯作者:
Ogawa K
影响因子:
2
作者:
Sharma MK;Imamichi S;Fukuchi M;Samarth RM;Tomita M;Matsumoto Y
通讯作者:
Matsumoto Y
影响因子:
8.8
作者:
Someya, M.;Sakata, K-I;Matsumoto, Y.;Kamdar, R. P.;Kai, M.;Toyota, M.;Hareyama, M.
通讯作者:
Hareyama, M.
影响因子:
--
作者:
Berlin A;Lalonde E;Sykes J;Zafarana G;Chu KC;Ramnarine VR;Ishkanian A;Sendorek DH;Pasic I;Lam WL;Jurisica I;van der Kwast T;Milosevic M;Boutros PC;Bristow RG
通讯作者:
Bristow RG