62 research outputs found
Data_Sheet_1_Combining UPLC/Q-TOF-MS/MS With Biological Evaluation for NF-κB Inhibitors in Uyghur Medicine Althaea rosea Flowers.docx
The Althaea rosea (Linn.) flower is a common plant that is often used to control inflammation in Uyghur ethnic medicine. However, its active ingredients remain uncertain and difficult to identify, severely limiting its use as a valuable crop. This paper aims to establish a rapid assay strategy for the integration of ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UPLC/Q-TOF-MS/MS) and a biologically active (NF-κB inhibitor) luciferase reporter detection system to explore various anti-inflammatory compounds of A. rosea (Linn.) flowers. Potential anti-inflammatory components were screened using the NF-κB activity assay system and simultaneously identified based on mass spectrometry data. Four structural types of NF-κB inhibitors (phenolic acid, hydroxycinnamic acid, flavonoid, and dihydroflavone) were identified. Further cytokine assays confirmed their potential anti-inflammatory effects as NF-κB inhibitors. Compared with traditional chromatographic separation, integrated UPLC/Q-TOF-MS/MS identification compounds, and biological activity verification are more convenient and more reliable. This strategy clearly demonstrates that fingerprinting based on MS data not only can identify unknown components but also is a powerful and useful tool for screening trace active ingredients directly from complex matrices. A. rosea (Linn.) exhibits great health and pharmaceutical value and may contribute to the development of new anti-inflammatory drugs.</p
Small-Molecule Fluorogenic Probe for the Detection of Mitochondrial Temperature <i>In Vivo</i>
Mitochondria, as energy factories,
participate in many metabolic
processes and play vital roles in cell life. Most human diseases are
caused by mitochondrial dysfunction, and mitochondrial temperature
is an important indicator of mitochondrial function. Despite the biological
importance of mitochondria, there are few tools for detecting changes
in mitochondrial temperature in living organisms. Here, we report
on a thermosensitive rhodamine B (RhB)-derived fluorogenic probe (RhBIV)
that enables fluorescent labeling of cell mitochondria at concentrations
as low as 1 μM. We demonstrate that this probe exhibits a temperature-dependent
response in cell mitochondria. Furthermore, in mice, it has a long
half-life (t1/2) and is primarily enriched
in the liver. This unique thermosensitive probe offers a simple, nondestructive
method for longitudinal monitoring of mitochondrial temperature both in vitro and in vivo to elucidate fundamental
physiological and pathological processes related to mitochondrial
function
Variations in the CO<sub>2</sub> concentrations over time (different elimination amounts).
Variations in the CO2 concentrations over time (different elimination amounts).</p
Variations in the peak elimination rate and time required to reach maximum elimination rate with the quantity of the elimination amount (different elimination amounts).
Variations in the peak elimination rate and time required to reach maximum elimination rate with the quantity of the elimination amount (different elimination amounts).</p
Variation in the CO elimination amount over time (different CO concentrations).
Variation in the CO elimination amount over time (different CO concentrations).</p
Variation in the CO elimination rate over time (different CO concentrations).
Variation in the CO elimination rate over time (different CO concentrations).</p
Variation in the concentration of CO over time (different CO concentrations).
Variation in the concentration of CO over time (different CO concentrations).</p
Image_1_ELAVL1 promotes prostate cancer progression by interacting with other m6A regulators.tiff
N6-Methyladenosine (m6A) imbalance is an important factor in the occurrence and development of prostate cancer (PCa). Many m6A regulators have been found to be significantly dysregulated in PCa. ELAVL1 is an m6A binding protein that can promote the occurrence and development of tumors in an m6A-dependent manner. In this study, we found that most m6A regulators were significantly dysregulated in PCa, and some m6A regulators were associated with the progression-free interval. Mutations and copy number variations of these m6A regulators can alter their expression. However, ELAVL1 mutations were not found in PCa. Nevertheless, ELAVL1 upregulation was closely related to PCa proliferation. High ELAVL1 expression was also related to RNA metabolism. Further experiments showed that ELAVL1 interacted with other m6A regulators and that several m6A regulatory mRNAs have m6A sites that can be recognized by ELAVL1. Additionally, protein–protein interactions occur between ELAVL1 and other m6A regulators. Finally, we found that the dysregulation of ELAVL1 expression occurred in almost all tumors, and interactions between ELAVL1 and other m6A regulators also existed in almost all tumors. In summary, ELAVL1 is an important molecule in the development of PCa, and its interactions with other m6A regulators may play important roles in PCa progression.</p
Table_1_ELAVL1 promotes prostate cancer progression by interacting with other m6A regulators.xlsx
N6-Methyladenosine (m6A) imbalance is an important factor in the occurrence and development of prostate cancer (PCa). Many m6A regulators have been found to be significantly dysregulated in PCa. ELAVL1 is an m6A binding protein that can promote the occurrence and development of tumors in an m6A-dependent manner. In this study, we found that most m6A regulators were significantly dysregulated in PCa, and some m6A regulators were associated with the progression-free interval. Mutations and copy number variations of these m6A regulators can alter their expression. However, ELAVL1 mutations were not found in PCa. Nevertheless, ELAVL1 upregulation was closely related to PCa proliferation. High ELAVL1 expression was also related to RNA metabolism. Further experiments showed that ELAVL1 interacted with other m6A regulators and that several m6A regulatory mRNAs have m6A sites that can be recognized by ELAVL1. Additionally, protein–protein interactions occur between ELAVL1 and other m6A regulators. Finally, we found that the dysregulation of ELAVL1 expression occurred in almost all tumors, and interactions between ELAVL1 and other m6A regulators also existed in almost all tumors. In summary, ELAVL1 is an important molecule in the development of PCa, and its interactions with other m6A regulators may play important roles in PCa progression.</p
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