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Structured Review

Shanghai GenePharma human integrin β1 sirna
Human Integrin β1 Sirna, supplied by Shanghai GenePharma, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human integrin β1 sirna/product/Shanghai GenePharma
Average 90 stars, based on 1 article reviews
human integrin β1 sirna - by Bioz Stars, 2026-03
90/100 stars

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A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. <t>Integrin</t> <t>β1</t> knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.
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Shanghai Genechem Ltd sirnas targeting the human integrin β1 gene
A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. <t>Integrin</t> <t>β1</t> knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.
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A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. <t>Integrin</t> <t>β1</t> knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.
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A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. <t>Integrin</t> <t>β1</t> knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.
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A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. <t>Integrin</t> <t>β1</t> knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.
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A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. Integrin β1 knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.

Journal: Oncotarget

Article Title: Matrix stiffness-mediated effects on stemness characteristics occurring in HCC cells

doi: 10.18632/oncotarget.8515

Figure Lengend Snippet: A. Increasing matrix stiffness upregulates the phosphorylation levels of Akt and mTOR, as well as the expressions of mTOR downstream molecules p-4E-BP and SOX2 in two HCC cells. B. Integrin β1 knockdown suppresses the phosphorylation level of Akt and mTOR, attenuates p-4E-BP and SOX2 expression in two HCC cells, while rapamycin, an mTOR-inhibitor, not only results in an obvious decrease of mTOR phosphorylation level and its downstream molecules expression, but also produces a slight increase in AKT phosphorylation level.

Article Snippet: Small interfering RNAs (siRNAs) targeting the human integrin β1 gene were designed by the Shanghai GeneChem, Co., Ltd., China.

Techniques: Expressing

Schematic diagram of the proposed mechanism by which matrix stiffness drives integrin β1/Akt/mTOR/SOX2 signaling pathway to regulate the stemness characteristics of HCC

Journal: Oncotarget

Article Title: Matrix stiffness-mediated effects on stemness characteristics occurring in HCC cells

doi: 10.18632/oncotarget.8515

Figure Lengend Snippet: Schematic diagram of the proposed mechanism by which matrix stiffness drives integrin β1/Akt/mTOR/SOX2 signaling pathway to regulate the stemness characteristics of HCC

Article Snippet: Small interfering RNAs (siRNAs) targeting the human integrin β1 gene were designed by the Shanghai GeneChem, Co., Ltd., China.

Techniques: