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recombinant FSH (FostiRel)

✓ Approved

Reliance Life Sciences Private Limited · FSHR · 重组蛋白

什么是 recombinant FSH?

recombinant FSH 是一种重组蛋白,由Reliance Life Sciences Private Limited研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Subcutaneous Injection。

药物档案

商品名FostiRel
公司Reliance Life Sciences Private Limited
药物类别重组蛋白
分子靶点FSHR
给药途径Injectable (Others), Subcutaneous Injection
状态Approved

作用机制

分子靶点

recombinant FSH 作用于 1 个分子靶点:

FSHRfollicle stimulating hormone receptor (FSHRO, ODG1)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

recombinant FSH 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Reproductive system and breast disordersInfertility female✓ Approved

相关研究文献

PubMedReproduction (Cambridge, England)2026-06-13

Asialoglycoprotein receptor-1 promotes hyperandrogenism in polycystic ovary syndrome through direct interaction with FSHR, leading to the cAMP-PKA-CREB pathway inhibition.

Liu Xitong X, Shi Juanzi J, Wang Ting T

Polycystic ovary syndrome (PCOS) is a prevalent multifactorial disorder characterized by hormone dysregulation and follicular development defects. Asialoglycoprotein receptor 1 (ASGR1), a C-type lectin predominantly expressed on the hepatic cell membrane, functions as a glycoprotein receptor that primarily mediates the binding, endocytosis and subsequent degradation of specific ligands. Notably, this receptor recognizes glycan moieties commonly carried by plasma glycoproteins-including glycoprotein hormones- and is thereby implicated in cellular signal transduction and material metabolism. In this study, we explored the potential association between ASGR1 and PCOS, and systematically explored its functional role and underlying mechanisms in PCOS pathogenesis. In vivo experiments showed that ovarian-specific overexpression of Asgr1 (AAV-Asgr1 mice) resulted in typical PCOS-like phenotypes. Mechanistically, we found that Asgr1-overexpression directly inhibited the activation of the cAMP/PKA/CREB signaling pathway-a key pathway mediating follicle-stimulating hormone (FSH)-regulated ovarian functions. Further in vitro and in vivo experiments revealed that ASGR1 exerted this effect at least in part by mediating the endocytosis and lysosomal degradation of FSH, thereby reducing subsequent downstream signaling activation. Conversely, the ovarian-specific knockdown of Asgr1 (AAV-sh-Asgr1 mice) showed a significant improvement in PCOS-related abnormalities.

PMID 42286817
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PubMedVirus genes2026-06-13

Reverse genetics strategies for coronaviruses: platform construction and applications in vaccine development.

Jia Yuhang Y, Han Xinyu X, Ma Yuchen Y, Wang Xinjuan X et al.

The continuous emergence of novel coronaviruses, characterized by high mutation rates and frequent recombination events, poses severe threats to global "One Health." Notably, the recent outbreak of the recombinant feline coronavirus (FCoV-23) and the persistence of SARS-CoV-2 variants underscore the urgent need to understand viral pathogenesis and cross-species transmission mechanisms. Reverse genetics technology serves as a critical platform for bridging genomic sequencing to functional virology, enabling targeted mutagenesis and the generation of recombinant viruses. However, the construction of reverse genetics systems for coronaviruses is often hampered by their exceptionally large genomes and the instability of viral cDNA sequences in bacterial hosts due to cytotoxicity. This review moves beyond a simple enumeration of methods to systematically compare current reverse genetics strategies-including in vitro ligation, bacterial artificial chromosome (BAC) systems, and transformation-associated recombination (TAR)-across different viral genera. Furthermore, we critically evaluate the application of these platforms in deciphering pathogenic mechanisms and developing next-generation vaccines, with a specific focus on overcoming technical bottlenecks and designing broad-spectrum countermeasures against emerging cross-species threats.

PMID 42286395
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PubMedAndrology2026-06-13

Clinical Outcomes of Orchiopexy and the Risk of Malignancy in Postpubertal Cryptorchid Patients.

Wu Xin X, Dong Biao B, Li Xiaotao X, Chen Rui R et al.

Postpubertal cryptorchidism remains clinically challenging, as patients often present with long-standing maldescent, impaired spermatogenesis, and an increased risk of testicular malignancy. However, the optimal management of this population remains controversial, and comprehensive data on clinical characteristics, surgical outcomes, endocrine changes, and spermatogenic damage are still limited. We conducted a single-center retrospective cohort study of 194 patients (210 undescended testes) undergoing primary orchiopexy between January 2018 and June 2024. Clinical characteristics, testicular position, ultrasonographic volume, semen parameters, endocrine parameters, and histopathology findings were collected. Intraoperative biopsies were obtained in 200 testes (95.2%) and graded using the Johnsen score. Severe spermatogenic impairment was defined as a Johnsen score ≤3; analyses of spermatogenic impairment were performed in 164 patients with available histological and endocrine assessments. Surgical outcomes were assessed in 185 testes with ≥3-month follow-up, and oncologic events were assessed in 155 patients (161 testes) with available follow-up data. Univariable and multivariable logistic regression analyses were performed to identify predictors of severe spermatogenic impairment. Most undescended testes were in a high position (196/210, 93.3%), and the affected testis had reduced volume in unilateral cases (median 6 vs. 18 mL). Overall anatomical success at 3 months was 80.0% (148/185), with recurrence and atrophy rates of 9.7% and 10.3%, respectively. Among patients with available semen data, unilateral cases showed no azoospermia, but 16 of 44 patients (36.4%) had at least one abnormality in sperm concentration, progressive motility, or normal morphology; by contrast, bilateral cases frequently presented with azoospermia or extremely low sperm counts. In unilateral cases, testosterone, LH, and FSH remained within the normal range without significant perioperative change; in bilateral cases, testosterone was generally preserved whereas FSH was elevated and remained above normal at follow-up. Histologically, only 17 of 200 biopsied testes (8.5%) had a Johnsen score >8, and 71/164 (43.3%) showed severe spermatogenic impairment. High testicular position was strongly associated with severe impairment (univariable OR 6.50, 95% CI 2.15-19.64, p < 0.001) and remained an independent predictor in multivariable analysis (adjusted OR 6.01, 95% CI 1.95-18.49, p = 0.002); affected testicular volume was independently inversely associated with severe impairment (adjusted OR 0.78 per 1 mL, 95% CI 0.64-0.95, p = 0.013). During a median follow-up of 54.6 months (range 12-78), one patient (0.5%) developed ipsilateral seminoma 48 months after orchiopexy. In postpubertal cryptorchidism, histological and functional spermatogenic impairment is often established before surgery and is unlikely to be substantially reversed by orchiopexy. The main value of orchiopexy lies in anatomical repositioning, pathological assessment, and facilitation of long-term surveillance. High testicular position and smaller preoperative testicular volume identify a subgroup at particularly high risk of severe spermatogenic failure, and malignancy risk is not eliminated, supporting the need for long-term follow-up.

PMID 42286960
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PubMedScientific reports2026-06-13

Defining functional puberty in female C57BL/6J mice using endocrine, cytological and morphological markers.

Chester Mélanie M, Wyckens Noalig N, Airaud Eloïse E, Corre Raphaël R et al.

Puberty marks the transition to reproductive competence and is driven by activation of the hypothalamo/pituitary/gonadal axis, culminating in first ovulation in females. In mice, puberty onset is commonly inferred from vaginal opening and estrous cyclicity, but the precise timing of first ovulation remains unclear. Here, we aimed to define reliable parameters of functional puberty in female C57BL/6J mice by integrating external, endocrine, and morphological measures. Vaginal opening and daily vaginal cytology were combined with daily serum luteinizing hormone (LH) and follicle-stimulating hormone (FSH) measurements and ovarian histology using the Pubertal Ovarian Maturation Score (Pub-Score), which estimates ovulation based on follicular development and corpus luteum morphology. Notably, we observed substantial inter-individual variability in puberty-related events, and no link between estrous cytology and first ovulation. Pub-Score analysis indicated that first ovulation occurred between 36 and 54 days postnatal, with a mean around 44 days, with no correlation with vaginal cytology. LH surges were detected in some of the females that had ovulated and showed limited temporal correspondence with vaginal cytology or Pub-Score estimates. Together, these findings demonstrate that puberty in female mice is a gradual, asynchronous process and that external or cytological markers alone are insufficient to define functional reproductive maturity.

PMID 42286056
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PubMedJournal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes2026-06-13

Female reproductive toxicity induced by nitrate in drinking water and the comparative ameliorative effects of ascorbic acid, curcumin and their combination.

Sharma Mona M, Kaur Navdeep N

The reproductive toxicity of nitrate in juvenile and adult female rats, and its amelioration with ascorbic acid, curcumin or their combination, was studied. Rats were classified into five groups: control, nitrate, nitrate + ascorbic acid, nitrate + curcumin, and nitrate + ascorbic acid + curcumin. Nitrate at 250 mg/L drinking water and ascorbic acid and curcumin at 100 mg/kg body weight were provided to rats via oral gavage for 42 days. Results showed a significant increase in malondialdehyde (MDA) level and decreases in activity of superoxide dismutase (SOD) and catalase (CAT); level of estrogen, progesterone, luteinizing hormone (LH) and follicle-stimulating hormone (FSH) in all treated groups of juvenile and adult rats, except for the group given a combination of both antioxidants. Glutathione peroxidase (GPx) activity decreased in the nitrate group of these rats. The number of atretic follicles increased and follicular diameter decreased in the nitrate group of juvenile and adult rats. A similar trend was also observed in juvenile rats given nitrate with ascorbic acid individually. In conclusion, nitrate caused higher toxicity in the ovaries of juveniles compared to adults. However, negative effects were reversed by amelioration with ascorbic acid and curcumin together, followed by curcumin and ascorbic acid separately.

PMID 42285372
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PubMedmAbs2026-06-13

Comparison of knockdown approaches for the generation of stable cell populations expressing afucosylated antibodies.

Tsachaki Maria M, Samy Andrew A, Peltret Mégane M, Brunstein Laplace Timothee T et al.

Targeted silencing of cellular genes in cell lines stably expressing a secreted recombinant protein offers a flexible and convenient strategy for modulating product quality attributes. However, unlike genetic knockout of a cellular gene or the use of potent inhibitors to eliminate cellular enzyme activity, gene knockdown approaches using microRNAs (miRNA) or short hairpin RNAs (shRNA) may result in only partial reduction of enzyme activity and only partial change of the desired product quality attribute. Moreover, through saturation of the Dicer pathway, shRNA may introduce cytotoxic effects that affect product yield. In this study, we demonstrate that miRNAs are a more suitable tool than shRNAs for α1,6-fucosyltransferase (FUT8) knockdown in Chinese hamster ovary (CHO) cells, when expressed under the control of an RNA-Polymerase II promoter. In the presence of miRNAs targeted to the FUT8 mRNA, the fucosylation levels of the N-glycan linked to Asn297 (EU numbering) of a recombinant monoclonal antibody (mAb) were considerably reduced (>90% afucosylation by hydrophilic interaction liquid chromatography - high‑performance liquid chromatography; no detectable fucosylated product by intact mass spectrometry), without a relevant impact on mAb expression. By comparison, overexpression of shRNAs targeted to the FUT8 mRNA resulted in higher levels of residual fucosylation of the mAb and a larger reduction in mAb titers. miRNAs overcame a limitation of the knockdown approach with shRNAs, making this approach a valuable tool for biopharmaceutical manufacturing.

PMID 42285912
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