Glioma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Therefore, it was hypothesized that the reduction in ACSL4 expression may have been involved in ferroptosis and proliferation in glioma.
|
31789401 |
2020 |
Septicemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, available clinical data indicate that levels of ACSL1 and ACSL4 induction was significantly higher in fatal cases of sepsis.
|
31681299 |
2019 |
Sepsis
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, available clinical data indicate that levels of ACSL1 and ACSL4 induction was significantly higher in fatal cases of sepsis.
|
31681299 |
2019 |
Colorectal Carcinoma
|
0.330 |
AlteredExpression
|
disease |
BEFREE |
Despite ACSL4 expression is upregulated progressively in CRC-like organoids, metformin is able to downregulate its expression, especially in the first two stages (I, II).
|
31339921 |
2019 |
Malignant neoplasm of breast
|
0.050 |
AlteredExpression
|
disease |
BEFREE |
The results presented in this manuscript demonstrated transcriptional mechanism is involved in the different expression of ACSL4 in human breast cancer cell lines of different aggressiveness.
|
31311992 |
2019 |
Breast Carcinoma
|
0.050 |
AlteredExpression
|
disease |
BEFREE |
The results presented in this manuscript demonstrated transcriptional mechanism is involved in the different expression of ACSL4 in human breast cancer cell lines of different aggressiveness.
|
31311992 |
2019 |
Triple Negative Breast Neoplasms
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
However, the upstream regulatory mechanisms leading to differential ACSL4 expression between triple negative breast cancer and ERα-positive cells remained unknown.
|
31311992 |
2019 |
Triple-Negative Breast Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
However, the upstream regulatory mechanisms leading to differential ACSL4 expression between triple negative breast cancer and ERα-positive cells remained unknown.
|
31311992 |
2019 |
Malignant Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
Recent studies revealed that ACSL4 is involved in biological responses including inflammation, steroidogenesis, cell death, female fertility, and cancer.
|
31306767 |
2019 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Recent studies revealed that ACSL4 is involved in biological responses including inflammation, steroidogenesis, cell death, female fertility, and cancer.
|
31306767 |
2019 |
Kidney Failure, Acute
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We observed that the Malondialdehyde (MDA) level was increased in dose-dependent manner similar to Acsl4 gene over expression suggesting a main role of ferroptosis in hemoglobinuria mediated AKI following envenomation.
|
30890325 |
2019 |
Gastrointestinal tract vascular insufficiency
|
0.010 |
Biomarker
|
disease |
BEFREE |
Ischemia-induced ACSL4 activation contributes to ferroptosis-mediated tissue injury in intestinal ischemia/reperfusion.
|
30737476 |
2019 |
Vascular insufficiency of intestine
|
0.010 |
Biomarker
|
disease |
BEFREE |
Ischemia-induced ACSL4 activation contributes to ferroptosis-mediated tissue injury in intestinal ischemia/reperfusion.
|
30737476 |
2019 |
Glioma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
The lower fatty acyl pool may be mediated by the lower protein expression levels of long-chain acyl-CoA synthetase 1 (ACSL1), ACSL4, and very long-chain acyl-CoA synthetase 3 (ACSVL3) in IDH1 mutant glioma.
|
30596429 |
2019 |
Intellectual Disability
|
0.160 |
Biomarker
|
group |
BEFREE |
As Drosophila Acsl and human ACSL4 are functionally conserved, our findings provide novel insights into a critical and previously unappreciated role of Acsl in neurogenesis and the pathogenesis of ACSL4-related ID.
|
30594466 |
2019 |
Malignant neoplasm of prostate
|
0.320 |
Biomarker
|
disease |
BEFREE |
In addition, ACSL4 has been associated to certain types of hormone resistance in prostate cancer.
|
30414939 |
2019 |
Malignant neoplasm of breast
|
0.050 |
Biomarker
|
disease |
BEFREE |
Acyl-CoA synthetase-4 is implicated in drug resistance in breast cancer cell lines involving the regulation of energy-dependent transporter expression.
|
30414939 |
2019 |
Breast Carcinoma
|
0.050 |
Biomarker
|
disease |
BEFREE |
Acyl-CoA synthetase-4 is implicated in drug resistance in breast cancer cell lines involving the regulation of energy-dependent transporter expression.
|
30414939 |
2019 |
Neoplasms
|
0.040 |
AlteredExpression
|
group |
BEFREE |
In sum, ACSL4 may be regarded as a novel therapeutic target regulating the expression of transporters involved in anticancer drug resistance through the mTOR pathway to restore drug sensitivity in tumors with poor prognosis for disease-free and overall survival.
|
30414939 |
2019 |
Prostate carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
In addition, ACSL4 has been associated to certain types of hormone resistance in prostate cancer.
|
30414939 |
2019 |
Degenerative polyarthritis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Particularly, the functional integrity of ABCD2 may play an important role in OA pathogenesis via the accumulation of VLCFAs and stimulation of apoptotic death through altering profiles of miRNAs that target ACSL4.
|
30264402 |
2018 |
Malignant Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
BMP4 was observed to be significantly overexpressed in the EGFR-TKI-resistant cells, and its mechanism of action was strongly associated with the induction of cancer cell energy metabolism through the modulation of Acyl-CoA synthetase long-chain family member 4.
|
30153566 |
2018 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
BMP4 was observed to be significantly overexpressed in the EGFR-TKI-resistant cells, and its mechanism of action was strongly associated with the induction of cancer cell energy metabolism through the modulation of Acyl-CoA synthetase long-chain family member 4.
|
30153566 |
2018 |
Malignant Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
Among the five family isoforms, ACSL1 and ACSL4 are able to promote ungoverned cell growth, facilitate tumor invasion and evade programmed cell death, while ACSL3 may have relatively complex functions in different types of cancer.
|
30008815 |
2018 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Among the five family isoforms, ACSL1 and ACSL4 are able to promote ungoverned cell growth, facilitate tumor invasion and evade programmed cell death, while ACSL3 may have relatively complex functions in different types of cancer.
|
30008815 |
2018 |