Masashi Okada

About Masashi Okada

Masashi Okada, With an exceptional h-index of 32 and a recent h-index of 23 (since 2020), a distinguished researcher at Yamagata University, specializes in the field of Cancer biology, Cancer stem cells, Metastasis, Invasion, Drug resistance.

His recent articles reflect a diverse array of research interests and contributions to the field:

Antagonizing MDM2 overexpression induced by MDM4 inhibitor CEP-1347 effectively reactivates wild-type p53 in malignant brain tumor cells

The Novel MDM4 Inhibitor CEP-1347 Activates the p53 Pathway and Blocks Malignant Meningioma Growth In Vitro and In Vivo

Domatinostat Targets the FOXM1–Survivin Axis to Reduce the Viability of Ovarian Cancer Cells Alone and in Combination with Chemotherapeutic Agents

Givinostat inhibition of sp1-dependent MGMT expression sensitizes glioma stem cells to temozolomide

HDAC class I inhibitor domatinostat preferentially targets glioma stem cells over their differentiated progeny

Gemcitabine cooperates with everolimus to inhibit the growth of and sensitize malignant meningioma cells to apoptosis induced by navitoclax, an inhibitor of anti-apoptotic bcl …

CEP-1347 targets MDM4 protein expression to activate p53 and inhibit the growth of glioma cells

Inhibition of the Phospholipase Cε–c-Jun N-Terminal Kinase Axis Suppresses Glioma Stem Cell Properties

Masashi Okada Information

University

Position

___

Citations(all)

3202

Citations(since 2020)

1605

Cited By

2395

hIndex(all)

32

hIndex(since 2020)

23

i10Index(all)

65

i10Index(since 2020)

53

Email

University Profile Page

Google Scholar

Masashi Okada Skills & Research Interests

Cancer biology

Cancer stem cells

Metastasis

Invasion

Drug resistance

Top articles of Masashi Okada

Antagonizing MDM2 overexpression induced by MDM4 inhibitor CEP-1347 effectively reactivates wild-type p53 in malignant brain tumor cells

Cancers

2023/8/30

Masashi Okada
Masashi Okada

H-Index: 21

The Novel MDM4 Inhibitor CEP-1347 Activates the p53 Pathway and Blocks Malignant Meningioma Growth In Vitro and In Vivo

Biomedicines

2023/7/12

Masashi Okada
Masashi Okada

H-Index: 21

Domatinostat Targets the FOXM1–Survivin Axis to Reduce the Viability of Ovarian Cancer Cells Alone and in Combination with Chemotherapeutic Agents

International Journal of Molecular Sciences

2023/6/28

Masashi Okada
Masashi Okada

H-Index: 21

Givinostat inhibition of sp1-dependent MGMT expression sensitizes glioma stem cells to temozolomide

Anticancer Research

2023/3/1

Masashi Okada
Masashi Okada

H-Index: 21

HDAC class I inhibitor domatinostat preferentially targets glioma stem cells over their differentiated progeny

International Journal of Molecular Sciences

2022/7/22

Masashi Okada
Masashi Okada

H-Index: 21

Gemcitabine cooperates with everolimus to inhibit the growth of and sensitize malignant meningioma cells to apoptosis induced by navitoclax, an inhibitor of anti-apoptotic bcl …

Cancers

2022/3/27

Masashi Okada
Masashi Okada

H-Index: 21

CEP-1347 targets MDM4 protein expression to activate p53 and inhibit the growth of glioma cells

Anticancer Research

2022/10/1

Masashi Okada
Masashi Okada

H-Index: 21

Inhibition of the Phospholipase Cε–c-Jun N-Terminal Kinase Axis Suppresses Glioma Stem Cell Properties

International Journal of Molecular Sciences

2022/8/7

Masashi Okada
Masashi Okada

H-Index: 21

Targeting folate metabolism is selectively cytotoxic to glioma stem cells and effectively cooperates with differentiation therapy to eliminate tumor-initiating cells in glioma …

International Journal of Molecular Sciences

2021/10/27

Masashi Okada
Masashi Okada

H-Index: 21

Lurasidone sensitizes cancer cells to osimertinib by inducing autophagy and reduction of survivin

Anticancer Research

2021/9/1

Masashi Okada
Masashi Okada

H-Index: 21

Dexamethasone sensitizes cancer stem cells to gemcitabine and 5-fluorouracil by increasing reactive oxygen species production through nrf2 reduction

Life

2021/8/27

Masashi Okada
Masashi Okada

H-Index: 21

Inhibition of the Lipid Droplet–Peroxisome Proliferator-Activated Receptor α Axis Suppresses Cancer Stem Cell Properties

Genes

2021/1/14

Masashi Okada
Masashi Okada

H-Index: 21

Inhibition of the lipid dropletperoxisome proliferator-activated receptor α axis suppresses cancer stem cell properties. Genes. 2021; 12: 99

2021

Gemcitabine radiosensitization primes irradiated malignant meningioma cells for senolytic elimination by navitoclax

Neuro-Oncology Advances

2021/1/1

Atsushi Sato
Atsushi Sato

H-Index: 12

Masashi Okada
Masashi Okada

H-Index: 21

Therapeutic targeting of pancreatic cancer stem cells by dexamethasone modulation of the MKP-1–JNK axis

Journal of Biological Chemistry

2020/12/25

Masashi Okada
Masashi Okada

H-Index: 21

Atsushi Sato
Atsushi Sato

H-Index: 12

Inhibition of retinoblastoma cell growth by CEP1347 through activation of the P53 pathway

Anticancer Research

2020/9/1

Masashi Okada
Masashi Okada

H-Index: 21

Doxazosin, a classic alpha 1-adrenoceptor antagonist, overcomes osimertinib resistance in cancer cells via the upregulation of autophagy as drug repurposing

Biomedicines

2020/8/5

Masashi Okada
Masashi Okada

H-Index: 21

Verteporfin inhibits oxidative phosphorylation and induces cell death specifically in glioma stem cells

The FEBS Journal

2020/5

Masashi Okada
Masashi Okada

H-Index: 21

See List of Professors in Masashi Okada University(Yamagata University)