Publications by authors named "Ikumi Soeda"

Article Synopsis
  • The study investigates the role of the platelet isoform of phosphofructokinase (PFKP) in breast cancer (BC), focusing on its expression levels and functions in cancer cells.
  • Researchers assessed PFKP expression in various BC and non-cancerous cell lines, discovering it was notably higher in certain aggressive BC types and correlated with other cancer-related genes.
  • Results showed that reducing PFKP levels decreased cell proliferation, invasiveness, and migration in multiple BC cell lines, suggesting that PFKP could be a potential new therapeutic target for treating breast cancer.
View Article and Find Full Text PDF

Background: Accumulating evidence indicates tumor-promoting roles of synaptotagmin 13 () in several cancers; however, no studies have investigated its expression in breast cancer (BC). This study aimed to clarify the significance of in BC.

Methods: mRNA expression levels were evaluated in BC cell lines.

View Article and Find Full Text PDF

Purpose: Papillary thyroid cancer (PTC) is generally associated with a favorable prognosis. However, some patients have fatal disease, with locally infiltrating tumors or progressive distant metastases; yet few studies have investigated the characteristics of the tumor-progressive gene expression profile in advanced PTC. We conducted this study to clarify the gene expression status in advanced PTC and identify candidate molecules for prognostic biomarkers.

View Article and Find Full Text PDF

Breast cancer (BC) is the most common malignant tumor in females. Development of novel biomarkers or therapeutic targets may contribute toward the improvement of a patient's prognosis. Marginal zone B and B1 cell-specific protein (MZB1) is an unfolded protein response-related chaperone and mainly exists in the endoplasmic reticulum of B lymphocytes, although little is known regarding its role in BC cells.

View Article and Find Full Text PDF

Context: Mutations in dual oxidase (DUOX2) have been proposed as a cause of congenital hypothyroidism. Previous reports suggest that biallelic mutations of DUOX2 cause permanent congenital hypothyroidism and that monoallelic mutations cause transient congenital hypothyroidism.

Objective: To clarify the inheritance of hypothyroidism, we looked at the DUOX2 gene in patients with transient congenital hypothyroidism.

View Article and Find Full Text PDF

A PHP Error was encountered

Severity: Notice

Message: fwrite(): Write of 34 bytes failed with errno=28 No space left on device

Filename: drivers/Session_files_driver.php

Line Number: 272

Backtrace:

A PHP Error was encountered

Severity: Warning

Message: session_write_close(): Failed to write session data using user defined save handler. (session.save_path: /var/lib/php/sessions)

Filename: Unknown

Line Number: 0

Backtrace: