High miR-21 expression from FFPE tissues is associated with poor survival and response to adjuvant chemotherapy in colon cancer.
High miR-21 expression from FFPE tissues is associated with poor survival and response to adjuvant chemotherapy in colon cancer.
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来自FFPE组织的高miR-21表达与结肠癌中辅助化疗的生存不良和对辅助化疗的反应有关。
DOI:
10.1002/ijc.28522
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发表时间:
2014-04-15
影响因子:
6.4
通讯作者:
Harris, Curtis C.
中科院分区:
文献类型:
--
作者:
Oue, Naohide;Anami, Katsuhiro;Schetter, Aaron J.;Moehler, Markus;Okayama, Hirokazu;Khan, Mohammed A.;Bowman, Elise D.;Mueller, Annett;Schad, Arno;Shimomura, Manabu;Hinoi, Takao;Aoyagi, Kazuhiko;Sasaki, Hiroki;Okajima, Masazumi;Ohdan, Hideki;Galle, Peter R.;Yasui, Wataru;Harris, Curtis C.
Colon cancer (CC) is a leading cause of cancer mortality. Novel biomarkers are needed to identify CC patients at high risk of recurrence and those who may benefit from therapeutic intervention. The aim of this study is to investigate if miR-21 expression from RNA isolated from formalin-fixed paraffin-embedded (FFPE) tissue sections is associated with prognosis and therapeutic outcome for patients with CC. The expression of miR-21 was measured by quantitative reverse transcriptase-polymerase chain reaction in a Japanese cohort (stage I–IV, n = 156) and a German cohort (stage II, n = 145). High miR-21 expression in tumors was associated with poor survival in both the stage II/III Japanese (P = 0.0008) and stage II German (P = 0.047) cohorts. These associations were independent of other clinical covariates in multivariable models. Receipt of adjuvant chemotherapy was not beneficial in patients with high miR-21 in either cohort. In the Japanese cohort, high miR-21 expression was significantly associated with poor therapeutic outcome (P = 0.0001) and adjuvant therapy was associated with improved survival in patients with low miR-21 (P = 0.001). These results suggest that miR-21 is a promising biomarker to identify patients with poor prognosis and can be accurately measured in FFPE tissues. The expression of miR-21 may also identify patients who will benefit from adjuvant chemotherapy.
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影响因子:
64.8
作者:
Lu, J;Getz, G;Golub, TR
通讯作者:
Golub, TR
影响因子:
3.5
作者:
Goswami RS;Waldron L;Machado J;Cervigne NK;Xu W;Reis PP;Bailey DJ;Jurisica I;Crump MR;Kamel-Reid S
通讯作者:
Kamel-Reid S
影响因子:
5
作者:
Hui, Angela B. Y.;Shi, Wei;Liu, Fei-Fei
通讯作者:
Liu, Fei-Fei
影响因子:
20.3
作者:
Rossi, Simona;Shimizu, Masayoshi;Calin, George A.
通讯作者:
Calin, George A.
影响因子:
5.3
作者:
Krichevsky AM;Gabriely G
通讯作者:
Gabriely G