+ |
perfluorooctane-1-sulfonic acid | up-regulates activity
chemical activation
|
ESR2 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268763 |
|
|
in vitro |
|
pmid |
sentence |
23764977 |
Seven PFCs [perfluorohexane sulfonate (PFHxS), perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), perfluorononanoate (PFNA), perfluorodecanoate (PFDA), perfluoroundecanoate (PFUnA), and perfluorododecanoate (PFDoA)] were analyzed in vitro for their potential to affect estrogen receptor (ER) and androgen receptor (AR) transactivity as well as aromatase enzyme activity. The PFCs were assessed as single compounds and in an equimolar mixture. PFHxS, PFOS and PFOA significantly induced the ER transactivity, whereas PFHxS, PFOS, PFOA, PFNA and PFDA significantly antagonized the AR activity in a concentration-dependent manner. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
perfluorooctane-1-sulfonic acid | up-regulates activity
chemical activation
|
PPARA |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268789 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
16731579 |
Human, mouse, and rat PPARα were activated by PFOA isomers and PFOS. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268754 |
|
|
Mus musculus |
|
pmid |
sentence |
34861291 |
Perfluorooctane sulfonate (PFOS) is a stable environmental contaminant that can activate peroxisome proliferator-activated receptor alpha (PPARα). These results indicate that mouse PPARα can be activated in the liver by PFOS causing increased expression of Acox1, Cyp4a10 and histopathological changes in the liver. |
|
Publications: |
2 |
Organism: |
Mus Musculus |
Tissue: |
Liver |
+ |
perfluorooctane-1-sulfonic acid | up-regulates activity
chemical activation
|
ESR1 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268760 |
|
|
in vitro |
|
pmid |
sentence |
23764977 |
Seven PFCs [perfluorohexane sulfonate (PFHxS), perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), perfluorononanoate (PFNA), perfluorodecanoate (PFDA), perfluoroundecanoate (PFUnA), and perfluorododecanoate (PFDoA)] were analyzed in vitro for their potential to affect estrogen receptor (ER) and androgen receptor (AR) transactivity as well as aromatase enzyme activity. The PFCs were assessed as single compounds and in an equimolar mixture. PFHxS, PFOS and PFOA significantly induced the ER transactivity, whereas PFHxS, PFOS, PFOA, PFNA and PFDA significantly antagonized the AR activity in a concentration-dependent manner. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
perfluorooctane-1-sulfonic acid | up-regulates activity
chemical activation
|
PPARD |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268757 |
|
|
in vitro |
|
pmid |
sentence |
31332417 |
In the present study, we demonstrated PFASs bound to and activated human PPARb/d-LBD directly. The PPARb/d binding potency and transcriptional activity of PFASs were all related to the carbon chain length and the terminal functional group. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
perfluorooctane-1-sulfonic acid | down-regulates activity
chemical inhibition
|
AR |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268767 |
|
|
in vitro |
|
pmid |
sentence |
23764977 |
Seven PFCs [perfluorohexane sulfonate (PFHxS), perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), perfluorononanoate (PFNA), perfluorodecanoate (PFDA), perfluoroundecanoate (PFUnA), and perfluorododecanoate (PFDoA)] were analyzed in vitro for their potential to affect estrogen receptor (ER) and androgen receptor (AR) transactivity as well as aromatase enzyme activity. The PFCs were assessed as single compounds and in an equimolar mixture. PFHxS, PFOS and PFOA significantly induced the ER transactivity, whereas PFHxS, PFOS, PFOA, PFNA and PFDA significantly antagonized the AR activity in a concentration-dependent manner. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
perfluorooctane-1-sulfonic acid | up-regulates activity
chemical activation
|
PPARG |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268787 |
|
|
Mus musculus |
3T3-L1 Cell |
pmid |
sentence |
16731579 |
Taken together, these data show that of the NRs studied, PPARα is the most likely target of PFOA and PFOS, although PPARγ is also activated to some extent. |
|
Publications: |
1 |
Organism: |
Mus Musculus |