Author/Authors :
Lo، نويسنده , , Hui-Wen and Hsu، نويسنده , , Sheng-Chieh and Ali-Seyed، نويسنده , , Mohamed and Gunduz، نويسنده , , Mehmet and Xia، نويسنده , , Weiya and Wei، نويسنده , , Yongkun and Bartholomeusz، نويسنده , , Geoffrey and Shih، نويسنده , , Jin-Yuan and Hung، نويسنده , , Mien-Chie، نويسنده ,
Abstract :
Summary
mal growth factor receptor (EGFR) exists in the nucleus of highly proliferative cells where it functions as a transcription factor. Although EGFR has transactivational activity, it lacks a DNA binding domain and, therefore, may require a DNA binding transcription cofactor for its transcriptional function. Here, we report that EGFR physically interacts with signal transducers and activators of transcription 3 (STAT3) in the nucleus, leading to transcriptional activation of inducible nitric oxide synthase (iNOS). In breast carcinomas, nuclear EGFR positively correlates with iNOS. This study describes a mode of transcriptional control involving cooperated efforts of STAT3 and nuclear EGFR. Our work suggests that the deregulated iNOS/NO pathway may partly contribute to the malignant biology of tumor cells with high levels of nuclear EGFR and STAT3.