General Information of the Ferroptosis Target (ID: TAR10004)
Target Name Long-chain-fatty-acid--CoA ligase 1 (ACSL1)
Synonyms
Acyl-CoA synthetase 1; Arachidonate--CoA ligase; Long-chain acyl-CoA synthetase 1; Long-chain acyl-CoA synthetase 2; Long-chain fatty acid-CoA ligase 2; Palmitoyl-CoA ligase 1; Palmitoyl-CoA ligase 2; Phytanate--CoA ligase
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Gene Name ACSL1
Sequence
MQAHELFRYFRMPELVDFRQYVRTLPTNTLMGFGAFAALTTFWYATRPKPLKPPCDLSMQ
SVEVAGSGGARRSALLDSDEPLVYFYDDVTTLYEGFQRGIQVSNNGPCLGSRKPDQPYEW
LSYKQVAELSECIGSALIQKGFKTAPDQFIGIFAQNRPEWVIIEQGCFAYSMVIVPLYDT
LGNEAITYIVNKAELSLVFVDKPEKAKLLLEGVENKLIPGLKIIVVMDAYGSELVERGQR
CGVEVTSMKAMEDLGRANRRKPKPPAPEDLAVICFTSGTTGNPKGAMVTHRNIVSDCSAF
VKATENTVNPCPDDTLISFLPLAHMFERVVECVMLCHGAKIGFFQGDIRLLMDDLKVLQP
TVFPVVPRLLNRMFDRIFGQANTTLKRWLLDFASKRKEAELRSGIIRNNSLWDRLIFHKV
QSSLGGRVRLMVTGAAPVSATVLTFLRAALGCQFYEGYGQTECTAGCCLTMPGDWTAGHV
GAPMPCNLIKLVDVEEMNYMAAEGEGEVCVKGPNVFQGYLKDPAKTAEALDKDGWLHTGD
IGKWLPNGTLKIIDRKKHIFKLAQGEYIAPEKIENIYMRSEPVAQVFVHGESLQAFLIAI
VVPDVETLCSWAQKRGFEGSFEELCRNKDVKKAILEDMVRLGKDSGLKPFEQVKGITLHP
ELFSIDNGLLTPTMKAKRPELRNYFRSQIDDLYSTIKV

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Family ATP-dependent AMP-binding enzyme family
Function
Catalyzes the conversion of long-chain fatty acids to their active form acyl-CoAs for both synthesis of cellular lipids, and degradation via beta-oxidation. Preferentially uses palmitoleate, oleate and linoleate. Preferentially activates arachidonate than epoxyeicosatrienoic acids (EETs) or hydroxyeicosatrienoic acids (HETEs).

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Gene ID 2180
Uniprot ID
P33121
Target Type Driver Suppressor Marker
Mechanism Diagram Click to View the Original Diagram
Tissue Relative Abundances of This Target
Full List of Regulator(s) of This Ferroptosis Target and Corresponding Disease/Drug Response(s)
ACSL1 can be involved in and affect the ferroptosis by the following regulators, and result in corresponding disease/drug response(s). You can browse corresponding disease or drug response(s) resulting from the regulation of certain regulators.
Browse Regulator related Disease
Browse Regulator related Drug
Protein arginine N-methyltransferase 1 (PRMT1)
Acute myeloid leukaemia [ICD-11: 2A60]
In total 1 item(s) under this disease
Experiment 1 Reporting the Ferroptosis-centered Disease Response of This Regulator [1]
Regulator for Ferroptosis Suppressor
Responsed Drug GSK3368715 Phase 1
Pathway Response Fatty acid metabolism hsa01212
Cell Process Cell ferroptosis
In Vitro Model
NB4 cells Acute promyelocytic leukemia Homo sapiens CVCL_0005
HEL cells Erythroleukemia Homo sapiens CVCL_0001
MOLM-13 cells Adult acute myeloid leukemia Homo sapiens CVCL_2119
HEK-293T cells Normal Homo sapiens CVCL_0063
In Vivo Model
5 x 106 NB4 cells were subcutaneously injected into the flank of 6-7-week-old female nude mice. The tumor number, body weight, and tumor volume were measured every other day. Tumor volumes were estimated using the following formula: tumor volume = (length x width2)/2. When tumor volumes reached 100-200 mm3, the mice were randomly divided into solvent control, RSL3, GSK3368715, or RSL3 + GSK3368715 combination groups (six mice per group). Specifically, for the RSL3 group, mice received intraperitoneal injections of RSL3 at 50 mg/kg 2 days apart. In the GSK3368715 group, GSK3368715 was intraperitoneally injected into mice at a dose of 75 mg/kg for 2 consecutive days per week. For the group that received RSL3 + GSK3368715 combination treatment, GSK3368715 (75 mg/kg) was administered by intraperitoneal injection for the first 2 days. Immediately thereafter, the mice received an intraperitoneal injection of RSL3 (50 mg/kg) 2 days apart. After 1 day of rest, the cycle was repeated until the end of the study on Day 21. Tumor volumes and body weights of the mice were measured and recorded every other day.

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Response Description Both GSK3368715 and PRMT1 knockout upregulated acyl-CoA synthetase long-chain family member 1 (ACSL1), which acts as a ferroptosis promoter by increasing lipid peroxidation. Knockout ACSL1 reduced the ferroptosis sensitivity of Acute myeloid leukemia (AML) cells following GSK3368715 treatment. Overall, PRMT1 inhibition promotes ferroptosis sensitivity via ACSL1 upregulation in acute myeloid leukemia.
Unspecific Regulator
Breast cancer [ICD-11: 2C60]
In total 1 item(s) under this disease
Experiment 1 Reporting the Ferroptosis-centered Disease Response of This Regulator [2]
Responsed Drug alpha-Eleostearic acid Investigative
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model
MDA-MB-468 cells Breast adenocarcinoma Homo sapiens CVCL_0419
MDA-MB-231 cells Breast adenocarcinoma Homo sapiens CVCL_0062
BT-20 cells Invasive breast carcinoma of no special type Homo sapiens CVCL_0178
BT-549 cells Invasive breast carcinoma Homo sapiens CVCL_1092
HCC38 cells Breast ductal carcinoma Homo sapiens CVCL_1267
HCC1806 cells Breast squamous cell carcinoma Homo sapiens CVCL_1258
HCC1187 cells Breast ductal carcinoma Homo sapiens CVCL_1247
HCC1143 cells Breast ductal carcinoma Homo sapiens CVCL_1245
HCC70 cells Breast ductal carcinoma Homo sapiens CVCL_1270
Hs-578T cells Invasive breast carcinoma Homo sapiens CVCL_0332
MCF-10A cells Normal Homo sapiens CVCL_0598
MCF-12A cells Normal Homo sapiens CVCL_3744
In Vivo Model
Mice were housed in a dedicated laboratory animal facility with 12-h light:dark cycle, at 70F+/-2 degrees, and 40-70% relative humidity. Orthotopic xenografts were generated by implanting 2.5 million MDA-MB-231 cells in 100 uL phosphate-buffered saline (PBS) mixed with 100 uL growth factor-reduced Matrigel (Corning) bilaterally into the fourth inguinal fat pad of four- to six-week-old female NOD.

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Response Description a-eleostearic acid (ESA)-triggered ferroptosis is mediated by acyl-CoA synthetase long-chain isoform 1 (ACSL1), which promotes ESA incorporation into neutral lipids including triacylglycerols in Breast adenocarcinoma.
Protein arginine N-methyltransferase 1 (PRMT1)
GSK3368715 [Phase 1]
In total 1 item(s) under this drug
Experiment 1 Reporting the Ferroptosis-centered Drug Response of This Regulator [1]
Regulator for Ferroptosis Suppressor
Responsed Disease Acute myeloid leukaemia [ICD-11: 2A60]
Pathway Response Fatty acid metabolism hsa01212
Cell Process Cell ferroptosis
In Vitro Model NB4 cells Acute promyelocytic leukemia Homo sapiens CVCL_0005
HEL cells Erythroleukemia Homo sapiens CVCL_0001
MOLM-13 cells Adult acute myeloid leukemia Homo sapiens CVCL_2119
HEK-293T cells Normal Homo sapiens CVCL_0063
In Vivo Model
5 x 106 NB4 cells were subcutaneously injected into the flank of 6-7-week-old female nude mice. The tumor number, body weight, and tumor volume were measured every other day. Tumor volumes were estimated using the following formula: tumor volume = (length x width2)/2. When tumor volumes reached 100-200 mm3, the mice were randomly divided into solvent control, RSL3, GSK3368715, or RSL3 + GSK3368715 combination groups (six mice per group). Specifically, for the RSL3 group, mice received intraperitoneal injections of RSL3 at 50 mg/kg 2 days apart. In the GSK3368715 group, GSK3368715 was intraperitoneally injected into mice at a dose of 75 mg/kg for 2 consecutive days per week. For the group that received RSL3 + GSK3368715 combination treatment, GSK3368715 (75 mg/kg) was administered by intraperitoneal injection for the first 2 days. Immediately thereafter, the mice received an intraperitoneal injection of RSL3 (50 mg/kg) 2 days apart. After 1 day of rest, the cycle was repeated until the end of the study on Day 21. Tumor volumes and body weights of the mice were measured and recorded every other day.

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Response Description Both GSK3368715 and PRMT1 knockout upregulated acyl-CoA synthetase long-chain family member 1 (ACSL1), which acts as a ferroptosis promoter by increasing lipid peroxidation. Knockout ACSL1 reduced the ferroptosis sensitivity of Acute myeloid leukemia (AML) cells following GSK3368715 treatment. Overall, PRMT1 inhibition promotes ferroptosis sensitivity via ACSL1 upregulation in acute myeloid leukemia.
Unspecific Regulator
alpha-Eleostearic acid [Investigative]
In total 1 item(s) under this drug
Experiment 1 Reporting the Ferroptosis-centered Drug Response of This Regulator [2]
Responsed Disease Breast cancer [ICD-11: 2C60]
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model MDA-MB-468 cells Breast adenocarcinoma Homo sapiens CVCL_0419
MDA-MB-231 cells Breast adenocarcinoma Homo sapiens CVCL_0062
BT-20 cells Invasive breast carcinoma of no special type Homo sapiens CVCL_0178
BT-549 cells Invasive breast carcinoma Homo sapiens CVCL_1092
HCC38 cells Breast ductal carcinoma Homo sapiens CVCL_1267
HCC1806 cells Breast squamous cell carcinoma Homo sapiens CVCL_1258
HCC1187 cells Breast ductal carcinoma Homo sapiens CVCL_1247
HCC1143 cells Breast ductal carcinoma Homo sapiens CVCL_1245
HCC70 cells Breast ductal carcinoma Homo sapiens CVCL_1270
Hs-578T cells Invasive breast carcinoma Homo sapiens CVCL_0332
MCF-10A cells Normal Homo sapiens CVCL_0598
MCF-12A cells Normal Homo sapiens CVCL_3744
In Vivo Model
Mice were housed in a dedicated laboratory animal facility with 12-h light:dark cycle, at 70F+/-2 degrees, and 40-70% relative humidity. Orthotopic xenografts were generated by implanting 2.5 million MDA-MB-231 cells in 100 uL phosphate-buffered saline (PBS) mixed with 100 uL growth factor-reduced Matrigel (Corning) bilaterally into the fourth inguinal fat pad of four- to six-week-old female NOD.

    Click to Show/Hide
Response Description a-eleostearic acid (ESA)-triggered ferroptosis is mediated by acyl-CoA synthetase long-chain isoform 1 (ACSL1), which promotes ESA incorporation into neutral lipids including triacylglycerols in Breast adenocarcinoma.
References
Ref 1 PRMT1 inhibition promotes ferroptosis sensitivity via ACSL1 upregulation in acute myeloid leukemia. Mol Carcinog. 2023 Aug;62(8):1119-1135. doi: 10.1002/mc.23550. Epub 2023 May 5.
Ref 2 Ferroptotic cell death triggered by conjugated linolenic acids is mediated by ACSL1. Nat Commun. 2021 Apr 14;12(1):2244. doi: 10.1038/s41467-021-22471-y.