Title : Histone deacetylase inhibitor OBP‑801 and amrubicin synergistically inhibit the growth of squamous cell lung carcinoma by inducing mitochondrial ASK1‑dependent apoptosis.

Pub. Date : 2020 Mar

PMID : 32124968






12 Functional Relationships(s)
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1 Histone deacetylase inhibitor OBP-801 and amrubicin synergistically inhibit the growth of squamous cell lung carcinoma by inducing mitochondrial ASK1-dependent apoptosis. YM753 compound mitogen-activated protein kinase kinase kinase 5 Homo sapiens
2 Histone deacetylase inhibitor OBP-801 and amrubicin synergistically inhibit the growth of squamous cell lung carcinoma by inducing mitochondrial ASK1-dependent apoptosis. amrubicin mitogen-activated protein kinase kinase kinase 5 Homo sapiens
3 The results demonstrated that a combined treatment with the potent histone deacetylase (HDAC) inhibitor OBP-801 and the third-generation anthracycline amrubicin synergistically inhibited the viability of SQCLC cell lines by inducing apoptosis signal-regulating kinase 1 (ASK1)-dependent, as well as JNK- and p38 mitogen-activated protein kinase (MAPK)-independent apoptosis. YM753 compound mitogen-activated protein kinase kinase kinase 5 Homo sapiens
4 The results demonstrated that a combined treatment with the potent histone deacetylase (HDAC) inhibitor OBP-801 and the third-generation anthracycline amrubicin synergistically inhibited the viability of SQCLC cell lines by inducing apoptosis signal-regulating kinase 1 (ASK1)-dependent, as well as JNK- and p38 mitogen-activated protein kinase (MAPK)-independent apoptosis. YM753 compound mitogen-activated protein kinase kinase kinase 5 Homo sapiens
5 The results demonstrated that a combined treatment with the potent histone deacetylase (HDAC) inhibitor OBP-801 and the third-generation anthracycline amrubicin synergistically inhibited the viability of SQCLC cell lines by inducing apoptosis signal-regulating kinase 1 (ASK1)-dependent, as well as JNK- and p38 mitogen-activated protein kinase (MAPK)-independent apoptosis. Anthracyclines mitogen-activated protein kinase kinase kinase 5 Homo sapiens
6 The results demonstrated that a combined treatment with the potent histone deacetylase (HDAC) inhibitor OBP-801 and the third-generation anthracycline amrubicin synergistically inhibited the viability of SQCLC cell lines by inducing apoptosis signal-regulating kinase 1 (ASK1)-dependent, as well as JNK- and p38 mitogen-activated protein kinase (MAPK)-independent apoptosis. Anthracyclines mitogen-activated protein kinase kinase kinase 5 Homo sapiens
7 The results demonstrated that a combined treatment with the potent histone deacetylase (HDAC) inhibitor OBP-801 and the third-generation anthracycline amrubicin synergistically inhibited the viability of SQCLC cell lines by inducing apoptosis signal-regulating kinase 1 (ASK1)-dependent, as well as JNK- and p38 mitogen-activated protein kinase (MAPK)-independent apoptosis. amrubicin mitogen-activated protein kinase kinase kinase 5 Homo sapiens
8 The results demonstrated that a combined treatment with the potent histone deacetylase (HDAC) inhibitor OBP-801 and the third-generation anthracycline amrubicin synergistically inhibited the viability of SQCLC cell lines by inducing apoptosis signal-regulating kinase 1 (ASK1)-dependent, as well as JNK- and p38 mitogen-activated protein kinase (MAPK)-independent apoptosis. amrubicin mitogen-activated protein kinase kinase kinase 5 Homo sapiens
9 OBP-801 treatment strongly induced the protein expression levels of thioredoxin-interacting protein (TXNIP), and amrubicin treatment increased the levels of intracellular reactive oxygen species (ROS), which suggested that this combination oxidized and dissociated thioredoxin 2 (Trx2) from mitochondrial ASK1 and activated ASK1. YM753 compound mitogen-activated protein kinase kinase kinase 5 Homo sapiens
10 OBP-801 treatment strongly induced the protein expression levels of thioredoxin-interacting protein (TXNIP), and amrubicin treatment increased the levels of intracellular reactive oxygen species (ROS), which suggested that this combination oxidized and dissociated thioredoxin 2 (Trx2) from mitochondrial ASK1 and activated ASK1. YM753 compound mitogen-activated protein kinase kinase kinase 5 Homo sapiens
11 OBP-801 treatment strongly induced the protein expression levels of thioredoxin-interacting protein (TXNIP), and amrubicin treatment increased the levels of intracellular reactive oxygen species (ROS), which suggested that this combination oxidized and dissociated thioredoxin 2 (Trx2) from mitochondrial ASK1 and activated ASK1. amrubicin mitogen-activated protein kinase kinase kinase 5 Homo sapiens
12 OBP-801 treatment strongly induced the protein expression levels of thioredoxin-interacting protein (TXNIP), and amrubicin treatment increased the levels of intracellular reactive oxygen species (ROS), which suggested that this combination oxidized and dissociated thioredoxin 2 (Trx2) from mitochondrial ASK1 and activated ASK1. amrubicin mitogen-activated protein kinase kinase kinase 5 Homo sapiens