Publications by authors named "Cheng-Fa Yeh"

Despite neoadjuvant chemoradiotherapy (CRT) being the established standard for treating advanced rectal cancer, clinical outcomes remain suboptimal, necessitating the identification of predictive biomarkers for improved treatment decisions. Previous studies have hinted at the oncogenic properties of the Fc fragment of IgG binding protein (FCGBP) in various cancers; however, its clinical significance in rectal cancer remains unclear. In this study, we first conducted an analysis of a public transcriptome comprising 46 rectal cancer patients.

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Replication stress converts the stalled forks into reversed forks, which is an important protection mechanism to prevent fork degradation and collapse into poisonous DNA double-strand breaks (DSBs). Paradoxically, the mechanism also acts in cancer cells to contribute to chemoresistance against various DNA-damaging agents. PARP1 binds to and is activated by stalled forks to facilitate fork reversal.

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Background: Cartilage acidic protein 1 (CRTAC1) is a glycosylated calcium-binding extracellular matrix protein. The oncological functions of CRTAC1 in urothelial carcinoma (UC) of the urinary bladder (UB) and upper urinary tract (UT) have not yet been elucidated. Based on the published UBUC transcriptome data, we re-evaluated the differential expression profile of calcium ion binding-related genes (GO:0005509), and we found that was the most significantly downregulated gene in UBUC progression.

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Nasopharyngeal carcinoma (NPC) is the most common malignant neoplasm of the nasopharynx. Despite improvements in the clinical treatment strategies for NPC, NPC patients usually have poor survival rates because of late diagnosis, tumor metastasis, and recurrence. Therefore, the identification of potential diagnostic and prognostic markers for NPC is imperative.

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Background: Concurrent chemoradiotherapy (CCRT) is suggested before resection surgery in the control of rectal cancer. Unfortunately, treatment outcomes are widely variable and highly patient-specific. Notably, rectal cancer patients with distant metastasis generally have a much lower survival rate.

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To reduce the risk of locoregional recurrence, the addition of neoadjuvant concurrent chemoradiotherapy (CCRT) is recommended before surgical management for rectal cancer patients. However, despite identical tumor histology, individual patient response to neoadjuvant CCRT varies greatly. Accordingly, a comprehensive molecular characterization that is used to predict CCRT efficacy is instantly needed.

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Article Synopsis
  • * Researchers studied the metabolic process of nucleobase-containing compounds in rectal adenocarcinoma patients and identified SLC28A2 as a key gene associated with resistance to CCRT.
  • * Strong SLC28A2 expression was linked to worse clinical outcomes, including decreased chances of tumor downstaging and lower survival rates, suggesting that it could serve as an unfavorable prognostic factor in these patients.
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Background: Nasopharyngeal carcinoma (NPC) is a malignant tumor originating from the nasopharynx with high morbidity and mortality in Southeast Asia and south of China. Roundabout guidance receptor 1 (ROBO1) can regulate axonogenesis (axon-like protrusion), which may play an important role in migration. However, the roles of ROBO1 in NPC have not been clarified.

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Nasopharyngeal carcinoma (NPC) is the most common malignant tumor in southern China and Southeast Asia. Although substantial research on NPC has been conducted, the resulting improvement in clinical outcomes remains very disappointing. NPC treatment typically involves radiation therapy and chemotherapy, but the high incidence of metastasis and recurrence in NPC patients result in poor survival.

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Article Synopsis
  • Nasopharyngeal carcinoma (NPC) is a lymphocyte-rich cancer from the nasopharynx that is sensitive to treatments but often recurs and spreads.
  • A study identified high expression levels of the SPIN4 gene as a key marker related to advanced disease status in NPC patients, suggesting poorer outcomes.
  • Analysis showed that increased SPIN4 expression correlates with worse survival rates and highlights its potential as a useful prognostic tool for NPC.
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We investigated the association of receptor tyrosine kinase-like orphan receptor 2 (ROR2) expression with clinicopathological features and oncologic outcomes in large urothelial carcinoma (UC) of the upper tract (UTUC) and urinary bladder (UBUC) cohorts. Through transcriptomic profiling of a published dataset (GSE31684), ROR2 was discovered to be the most upregulated gene during UC progression, focusing on the JNK cascade (GO:0007254). Initially, the evaluation of mRNA expression in 50 frozen UBUCs showed significantly upregulated levels in high-stage UC.

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The introduction of preoperative concurrent chemoradiotherapy (CCRT) increases the rate of anal preservation and allows tumor downstaging for clinical stage T3/T4 or node-positive rectal cancer patients. However, there is no precise predictive tool to verify the presence of residual tumor apart from surgical resection. The gastrointestinal (GI) tract not only digests nutrients but also coordinates immune responses.

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For locally advanced rectal cancer patients, introducing neoadjuvant concurrent chemoradiotherapy (CCRT) before radical resection allows tumor downstaging and increases the rate of anus retention. Since accurate staging before surgery and sensitivity prediction to CCRT remain challenging, a more precise genetic biomarker is urgently needed to enhance the management of such situations. The epithelial mucous barrier can protect the gut lumen, but aberrant mucin synthesis may defend against drug penetration.

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Article Synopsis
  • Neoadjuvant concurrent chemoradiotherapy (CCRT) may help rectal cancer patients, but predicting outcomes is tough, highlighting the need for biomarkers to customize treatments.
  • Researchers analyzed a dataset and identified the gene FRMD3 as a key factor linked to resistance against CCRT in rectal cancer patients.
  • High levels of FRMD3 expression were found to correlate with worse tumor status, increased metastasis, and poorer survival rates, suggesting it could be a valuable prognostic indicator for these patients.
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  • Cancer immunotherapy has become a key strategy for treating cancer, but it faces challenges like poor targeting and side effects that limit its clinical effectiveness.
  • Researchers are exploring new methods, particularly nano-immunotherapy, which utilizes nanoparticles to enhance the delivery and effectiveness of immunotherapeutic agents while minimizing side effects.
  • The review discusses the role of nanoparticles as carriers for these agents and how they can also function as direct immunomodulators to improve antitumor activity and patient survival rates.
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