Publications by authors named "I-Ching Lu"

Article Synopsis
  • Combination therapies using curcumin with cisplatin/carboplatin and gemcitabine can enhance cancer cell death in bladder cancer by inducing apoptosis and autophagy through suppression of Aurora A and activation of MEK/ERK.
  • Animal studies showed that this combination therapy reduced tumor growth in mice, linked to specific changes in protein expression within tumors.
  • Interestingly, while reduced Aurora A levels may not significantly impact drug sensitivity, high Aurora A expression in early-stage bladder cancer suggests that targeting it alongside promoting autophagy could improve treatment outcomes.
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We have previously identified a novel protein kinase, pk146, in the brain of Tetraodon. In the present study, we cloned the homologous protein kinase gene encoding a protein of 385 amino acid residues from zebrafish. The overall amino acid sequence and the kinase domain of zebrafish BSK146 shows 48% and 69% identity to that of rat sbk, a SH3-containing serine/threonine protein kinase.

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Heparin-binding neurotrophic factor (HBNF) is a secreted heparin-binding protein containing highly basic and cysteine-rich amino acid residues. In this study, we cloned the full-length HBNF cDNA from zebrafish and determined its genomic structure by bioinformatics analysis. Zebrafish HBNF gene is composed of five exons and four introns spanning approximately 82kb.

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The genomic structure of Tetraodon fluviatilis L29 gene was determined and its promoter activity was analyzed in COS-1 cells and zebrafish embryos. The TfL29 gene comprises four exons and three introns, spanning approximately 1.7kb.

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The BH3-only proapoptotic protein, BAD, was cloned from zebrafish embryos and its properties were characterized. Zebrafish BAD (zBAD) is a protein with 147 amino acids that contains a BH3 domain and a putative 14-3-3 binding site with the sequence of RPRSRS(84)AP, corresponding to S(136) in mouse BAD (mBAD). zBAD shares 34%, 28%, and 29% amino acid sequence identity to the human, mouse, and rat BAD, respectively.

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