Newly synthesized anticancer drug HUHS1015 is effective on malignant pleural mesothelioma

@article{Kaku2014NewlySA,
  title={Newly synthesized anticancer drug HUHS1015 is effective on malignant pleural mesothelioma},
  author={Yoshiko Kaku and Hisao Nagaya and Ayako Tsuchiya and Takeshi Kanno and Akinobu Gotoh and Akito Tanaka and Tadashi Shimizu and Syuhei Nakao and Chiharu Tabata and Takashi Nakano and Tomoyuki Nishizaki},
  journal={Cancer Science},
  year={2014},
  volume={105},
  pages={883 - 889}
}
The newly synthesized naftopidil analogue HUHS1015 reduced cell viability in malignant pleural mesothelioma cell lines MSTO‐211H, NCI‐H28, NCI‐H2052, and NCI‐H2452, with the potential greater than that for the anticancer drugs paclitaxel or cisplatin at concentrations higher than 30 μM. HUHS1015 induced both necrosis and apoptosis of MSTO‐211H and NCI‐H2052 cells. HUHS1015 upregulated expression of mRNAs for Puma, Hrk, and Noxa in MSTO‐211H and NCI‐H2052 cells, suggesting HUHS1015‐induced… 

The newly synthesized anticancer drug HUHS1015 is useful for treatment of human gastric cancer

The results of the present study show that HUHS1015 induces caspase-independent and casp enzyme-dependent apoptosis of MKN28 and MKN45 human gastric cancer cells, respectively, and effectively suppresses MKN 45 cell proliferation.

Curcumin induces apoptosis and inhibits angiogenesis in murine malignant mesothelioma

Curcumin may be potent enough to be developed as a novel therapeutic agent for the treatment of MPM after it was suggested that curcumin-induced cell apoptosis occurred via the mitochondrial pathway, and caspase-independent and AIF-dependent pathways.

Novel platinum agents and mesenchymal stromal cells for thoracic malignancies: state of the art and future perspectives

Mesenchymal stromal cells are a new promising tool in oncology and—although not yet utilized in the clinical practice, the authors think they will represent another main tool for cancer therapy and will probably play a leading role in the field of nanovectors and molecular medicine.

Possible new therapeutic agents for malignant pleural mesothelioma: anti-CD26 monoclonal antibody and naftopidil

It is shown that vascular endothelial growth factor (VEGF) is a key trigger of tumor angiogenesis in MPM, and therefore VEGF-targeting therapy may improve treatment outcomes, and mesothelin is an attractive target in the treatment of mesothelioma.

Repurposed Drugs in Gastric Cancer

This review explores GC and the different drugs repurposed for this disease, which is one of the major causes of death worldwide and the fourth leading cause of cancer mortality in 2020.

1-[2-(2-Methoxyphenylamino)ethylamino]-3-(naphthalene-1-yloxy)propan-2-ol May Be a Promising Anticancer Drug

HUHS1015 effectively suppresses tumor growth in mice inoculated with NCI-H2052, MKN45, or CW2 cells, with a potential similar to or higher than that of currently used anticancer drugs.

Naftopidil reduced the proliferation of lung fibroblasts and bleomycin‐induced lung fibrosis in mice

Histological and micro‐computed tomography examination revealed that naftopidil attenuated lung fibrosis and decreased serum surfactant protein‐D levels in bleomycin‐induced lung Fibrosis in mice, suggesting nafto‐2ʹ‐deoxyuridine may have therapeutic effects on Lung fibrosis.

Drug Repositioning of the α1-Adrenergic Receptor Antagonist Naftopidil: A Potential New Anti-Cancer Drug?

Naftopidil appears to display anti-cancer properties on different cancer types and could be considered as a candidate for drug repurposing although its anti- cancerous activities need to be studied more deeply in prospective randomized clinical trials.

Use of Anti-Noxa Antibody for Differential Diagnosis between Epithelioid Mesothelioma and Reactive Mesothelial Hyperplasia

Noxa mRNA expression levels were found to be increased in EM when compared to RMH by RT-PCR array analysis, and would be a valuable addition to the current antibody panel used for the differential diagnosis of EM and RMH.

Repositioned alpha-1 adrenoceptor blockers as anti-tumor drugs

References

SHOWING 1-10 OF 13 REFERENCES

Naftopidil induces apoptosis in malignant mesothelioma cell lines independently of α1-adrenoceptor blocking.

Naftopidil, as well as prazosin, has the potential to induce apoptosis in malignant mesothelioma cells by activating caspase-8 and the effector caspases-3, regardless of α1-adrenoceptor blocking.

nab-Paclitaxel mechanisms of action and delivery.

  • D. Yardley
  • Biology, Chemistry
    Journal of controlled release : official journal of the Controlled Release Society
  • 2013

The Winning Formulation: The Development of Paclitaxel in Pancreatic Cancer

In the era of biologic and molecularly targeted agents, the success of nab-paclitaxel in recalcitrant pancreatic cancer is a timely reminder of the importance and relevance of pharmacology and novel drug delivery technology in the development of anticancer drugs.

Role of Bcl‐2 in tumour cell survival and implications for pharmacotherapy

This discussion paper focuses primarily on anti‐apoptotic Bcl‐2, its activation in cancer, the manner in which it regulates the intrinsic and extrinsic mechanisms of apoptosis, and its broad molecular interactions with other critical proteins in the cell.

Patient selection and targeted treatment in the management of platinum-resistant ovarian cancer

Selecting the right patients through biomarker screening will help tailor therapy to patients and decrease superfluous treatment to those who are biomarker negative; this approach should lead to improved clinical results and decreased toxicities.

Tumor Delivery of Chemotherapy Combined with Inhibitors of Angiogenesis and Vascular Targeting Agents

This review looks at recent progress and the own preclinical experience in combining angiogenesis inhibitors, mainly acting on VEGF/VEGFR pathways, and vascular targeting agents with conventional chemotherapy, discussing the factors that determine the outcome of these treatments.

Phases of apoptosis of melanoma cells, but not of normal melanocytes, differently affect maturation of myeloid dendritic cells.

A novel mechanism of tumor escape that may prevent the development of antitumor immunity through the maturation block induced in DCs by neoplastic cells in the early phase of apoptosis is suggested.

1-[2-(2-Methoxyphenylamino)ethylamino]-3-(naphthalene-1-yloxy)propan-2-ol as a Potential Anticancer Drug

The results of the present study indicate that HUHS1015 induces apoptosis in a variety of cancer cells, possibly by activating caspase-4 and the effector caspases-3.

Protease Involvement in Fodrin Cleavage and Phosphatidylserine Exposure in Apoptosis*

A detailed kinetic analysis of three extranuclear end points of apoptosis, phosphatidylserine exposure, α-fodrin degradation, and plasma membrane blebbing, was performed and compared with nuclear