Publications by authors named "Shi-shuai Wen"

Article Synopsis
  • Papillary thyroid cancer (PTC) with the BRAF mutation leads to worse outcomes, and while BRAF inhibitors may help, drug resistance limits their effectiveness; this study explores how BRAF and DRP1 affect PTC cellular processes including growth and glucose metabolism.
  • The research shows that the BRAF mutation boosts aerobic glycolysis by activating the BRAF/p-ERK/p-DRP1(Ser616) pathway, which enhances cell division and reduces cell death, contributing to the cancer’s aggressiveness.
  • The study suggests that combining a glucose inhibitor (2-DG) with the BRAF inhibitor (dabrafenib) can significantly slow the progression of BRAF-positive PTC, indicating a promising new treatment strategy
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Context: Programmed cell death protein-1 (PD-1), cytotoxic T-lymphocyte antigen 4 (CTLA-4), T-cell immunoglobulin and mucin-domain containing-3 (TIM-3), lymphocyte activation gene-3 (LAG-3), and T-cell immunoglobulin and ITIM domain (TIGIT) are considered major immune co-inhibitory receptors (CIRs) and the most promising immunotherapeutic targets in cancer treatment, but they are largely unexplored in medullary thyroid carcinoma (MTC).

Objective: We aimed to provide the first evidence regarding the expression profiles and clinical significance of CIRs in a large cohort of MTC patients.

Design And Patients: In total, 200 MTC patients who received initial surgery in our hospital were included.

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Sporadic medullary thyroid carcinoma (MTC) is a relatively uncommon neuroendocrine malignancy and the molecular tumorigenesis of its sporadic type (sMTC) is only partially understood. In this study, we performed a study focusing on the genomic and transcriptomic characterization of sMTC. Twenty-nine sMTC patients were included.

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Background: Papillary thyroid cancer (PTC) has a strong propensity to metastasize to the cervical lymph nodes. Little was known currently about whether tumor's location would influence the risk of lymph node metastasis in PTC.

Methods: The study enrolled PTC patients who underwent primary surgical therapy in our center for small unifocal tumor.

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Article Synopsis
  • - Warburg discovered that tumor cells rely heavily on glycolysis for energy, even when oxygen is available, a phenomenon called the 'Warburg effect', but recent findings suggest that metabolic changes in cancer cells are more complex than he initially thought.
  • - Thyroid cancer, a common type of endocrine tumor, has shown notable metabolic changes in recent research, leading to ongoing clinical trials for drugs that target these metabolic pathways.
  • - The article aims to explore the metabolic alterations in thyroid cancer to identify potential biomarkers for prognosis and therapeutic targets, emphasizing the importance of further studies to validate these findings.
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Differentiated thyroid cancer (DTC) is associated with the highest propensity for lymph node metastases, given the significant morbidity associated with sacrificing the spinal accessory nerve, surgeons increasingly looked to minimizing functional deficits while maintaining oncologic outcome. We have detailed the technique of a selective neck dissection with more attention to preserving the cervical sensory nerves since 1999 in Fudan University Shanghai Cancer Center. We found that the radical dissection with preservation of the cutaneous branches including the great auricular nerve, the less occipital nerve and the supraclavicular nerve can maximally decrease the complications of paresthesia and dysesthesia postoperatively in the lower neck, the shoulders and the area around the ear in DTC cases when indications were allowed.

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Benefits of subdividing small-differentiated thyroid carcinoma (sDTC) by tumor size are controversial. We conducted a meta-analysis to investigate whether tumor size is associated with prognosis of sDTC. PubMed and Web of Science databases were searched from their inception to September 2018.

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Protein tyrosine phosphatases have diverse substrate specificities and intrinsic activities that lay the foundations for the fine-tuning of a phosphorylation network to precisely regulate cellular signal transduction. All classical PTPs share common catalytic mechanisms, and the important catalytic residues in the first sphere of their active sites have been well characterized. However, little attention has been paid to the second-sphere residues that are potentially important in defining the intrinsic activity and substrate specificity of PTPs.

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