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Downregulation of ERBB3 decreases the proliferation, migration and invasion of cervical cancer cells though the interaction with MTK‑1

机译：虽然与MTK-1的相互作用，ERBB3的下调降低了宫颈癌细胞的增殖，迁移和侵袭

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Jingyun Du; Shihua Zhou; Li Wang; Mulan Yu; Liyan Mei;
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1. Downregulation of ERBB3 decreases the proliferation, migration and invasion of cervical cancer cells though the interaction with MTK-1 [J] . Du Jingyun, Zhou Shihua, Wang Li, Oncology letters . 2018,第3aPta2期

机译：ErbB3的下调降低了宫颈癌细胞的增殖，迁移和侵袭，尽管与MTK-1的相互作用
2. Downregulation of HMGB1 by miR-34a is sufficient to suppress proliferation, migration and invasion of human cervical and colorectal cancer cells [J] . Chandrasekaran Karthik Subramanian, Sathyanarayanan Anusha, Karunagaran Devarajan Tumour biology : . 2016,第10期

机译：miR-34a对HMGB1的下调足以抑制人宫颈癌和结肠直肠癌细胞的增殖，迁移和侵袭
3. Downregulation of annexin A7 decreases proliferation, migration, and invasion of gastric cancer cells by reducing matrix metalloproteinase 1 and 9 expression [J] . Hu-Fang Yuan, Yong Li, Wei-Hua Ye, American Journal of Translational Research . 2019,第5期

机译：膜联蛋白A7的下调通过减少基质金属蛋白酶1和9的表达减少胃癌细胞的增殖，迁移和侵袭
4. Ablation of CD44 Decreases Cell Proliferation, Migration and Invasion via Down-Regulation of c-Src Transcription [C] . KeeSoo Nam, SeungAh Yoo, Kyung-Min Lee, Molecular Medicine TRI-CON. . 2014

机译：CD44的消融通过C-SRC转录的下调降低细胞增殖，迁移和侵袭
5. Abrogation of PIK3CA or PIK3R1 reduces proliferation, migration, and invasion in glioblastoma multiforme cells. [D] . Weber, Genevieve L. 2011

机译：废除PIK3CA或PIK3R1可减少多形性胶质母细胞瘤细胞的增殖，迁移和侵袭。
6. Downregulation of ERBB3 decreases the proliferation migration and invasion of cervical cancer cells though the interaction with MTK-1 [O] . Jingyun Du, Shihua Zhou, Li Wang, -1

机译：ERBB3的下调通过与MTK-1的相互作用降低了宫颈癌细胞的增殖迁移和侵袭
7. Downregulation of N-Acetylglucosaminyltransferase GCNT3 by miR-302b-3p Decreases Non-Small Cell Lung Cancer (NSCLC) Cell Proliferation, Migration and Invasion [O] . Qian Li, Pengzhan Ran, Xiyu Zhang, 2018

机译：MIR-302B-3P的N-乙酰甘氨酸氨基氨基氨基转移酶GCNT3的下调降低了非小细胞肺癌（NSCLC）细胞增殖，迁移和侵袭

Downregulation of ERBB3 decreases the proliferation, migration and invasion of cervical cancer cells though the interaction with MTK‑1

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