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Advances in the Impact of ASS1 Dysregulation on Metabolic Reprogramming of Tumor Cells
Cellular SignallingASS1(argininosuccinate synthase 1) is a rate-limiting enzyme in the urea cycle, catalyzing the synthesis of argininosuccinate from citrulline and aspartate to ultimately produce arginine and support cellular metabolism. Increasing evidence suggests that ASS1 is commonly dysregulated in the tumor microenvironment, promoting tumor cell metastasis and ...
Asif Shahzad, Zhuoran Teng, Jiaojiao Xia
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Spinosyn A derivatives as ASS1 activators and tumor inhibitors
Bioorganic & Medicinal Chemistry LettersSpinosad, a natural-origin pesticide, is extensively employed in agriculture and public health. Its primary component, Spinosyn A, has also attracted considerable interest due to its antiproliferative activity against various cancer cell lines. While ASS1 has emerged as a promising target for anticancer therapy, the development of ASS1 activators ...
Xin-Yu, Huang +8 more
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Arginine deprivation for ASS1-deficient mesothelioma
The Lancet Oncology, 2016www.thelancet.com/oncology Vol 17 October 2016 e423 Arginine deprivation therapy improves progression-free survival in patients with argininosuccinate synthetase 1 (ASS1)-defi cient malignant pleural mesothelioma, according to a new study . The investigators in the phase 2 trial screened 201 patients with mesothelioma from centres in the UK.
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Polymorphic Variants of ASS1 Gene Related to Arginine Metabolism and the Risk of HCC
Protein & Peptide Letters, 2023Background: Hepatocellular carcinoma is a primary liver cancer and 6th most common cancer globally. Inefficient diagnostic strategies and the limited availability of treatments are the foremost reasons. Variable factors directly impact the disease burden, among them, molecular alterations have been found to play a significant role.
Kulsoom Bibi +5 more
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ASS1 Deficiency Is Associated With Impaired Neuronal Differentiation in Zebrafish Larvae
Citrullinemia type 1 (CTLN1) is a rare autosomal recessive urea cycle disorder caused by deficiency of the cytosolic enzyme argininosuccinate synthetase 1 (ASS1) due to pathogenic variants in the ASS1 gene located on chromosome 9q34.11. Even though hyperammenomia is considered the major pathomechanistic factor for neurological impairment and cognitive ...
Stefan Kolker +2 more
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99 Chinese ASS1 Carriers: Genetics, Metabolism, and Citrulline Levels
Clinica Chimica ActaCitrullinemia type I is an autosomal recessive disorder caused by mutations in the ASS1 gene, whereas ASS1 mutation carriers typically have a mutation in only one allele. While carriers are usually asymptomatic, they often show mildly elevated plasma citrulline levels.
Lingwei HU, Xinwen Huang, Zhenzhen Hu
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2016
Glioblastoma multiforme (GBM) are the most common and most malignant brain tumours. Despite treatment advances, average survival remains unacceptably low with 15-months, hence novel therapies are desperately needed. Cellular metabolism plays a central role in cancers. Sensitivity towards arginine-deprivation via pegylated arginine deaminase (ADI-PEG20)
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Glioblastoma multiforme (GBM) are the most common and most malignant brain tumours. Despite treatment advances, average survival remains unacceptably low with 15-months, hence novel therapies are desperately needed. Cellular metabolism plays a central role in cancers. Sensitivity towards arginine-deprivation via pegylated arginine deaminase (ADI-PEG20)
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Mutation spectrum of the ASS1 gene in Korean patients with citrullinemia type I
Clinical Biochemistry, 2013Citrullinemia type I is a rare metabolic disorder and the distribution of mutations in the ASS1 gene varies among ethnic groups. We aimed to determine the molecular characteristics of citrullinemia type I in Korean patients.Biochemical and clinical findings were investigated and mutations in the ASS1 gene were identified using direct sequencing method ...
Hye In, Woo +9 more
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The Mechanism of TRIM21 Inhibiting the Invasion and Migration of ccRCC by Stabilizing ASS1
Molecular CarcinogenesisABSTRACTClear cell renal cell carcinoma (ccRCC) is characterized by its aggressive invasion and metastasis, presenting significant clinical challenges. Gaining insights into the molecular mechanisms underlying its progression is crucial for the development of effective therapeutic strategies.
Zhe Yang +11 more
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FoxO transcription factors regulate urea cycle through Ass1
Biochemical and Biophysical Research CommunicationsWhen amino acids are plentiful in the diet, the liver upregulates most enzymes responsible for amino acid degradation. In particular, the activity of urea cycle enzymes increases in response to high-protein diets to facilitate the excretion of excess nitrogen.
Samia Karkoutly +13 more
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