Subhayan Das
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Subhayan Das has a total of 134 co-authors. Here are the top co-authors by number of shared publications:
- Mahitosh Mandal
Indian Institute of Technology Kharagpur
25 shared publications Mahitosh Mandal
8 shared publications- Angana Biswas
School of Medical Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur 721302, India
7 shared publications Deblina Bharadwaj
Indian Institute of Technology Kharagpur
7 shared publications- Moumita Kundu
Department of Pharmaceutical Technology, Brainware University, Barasat, India
7 shared publications - Yetirajam Rajesh
School of Medical Science and Technology, Indian Institute of Technology, Kharagpur, West Bengal 721302, India
7 shared publications
Latest Publications
- 13 February 2025
- Published by Springer Nature in Cancer and Metastasis Reviews
- Vol. 44 (1) , 32
CTGF (CCN2): a multifaceted mediator in breast cancer progression and therapeutic targeting
Breast cancer, with its diverse subtypes like ER-positive, HER-2-positive, and triple-negative, presents complex challenges demanding personalized treatment approaches. The intricate interplay of genetic, environmental, and lifestyle factors underscores its status as a primary contributor to cancer-related fatalities in women globally. Understanding the molecular drivers specific to each subtype is crucial for developing effective therapies. In this landscape, connective tissue growth factor (CTGF), also referred to as cellular communication network factor 2 (CCN2), emerges as a significant player. CTGF regulates critical biological activities like cell growth, invasion, and migration, impacting breast cancer development and progression. It modulates breast tumor microenvironment by promoting angiogenesis, activating cancer-associated fibroblasts (CAFs), and inducing inflammation. The activity of CTGF depends on several factors including oxygen levels, hormone signals, and growth factors and differs according to the type of breast cancer. CTGF can regulate breast cancer cells by activating various signaling pathways and modulating the transcription of other genes that are involved in tumor development and metastasis including S100A4, glucose transporter 3 (GLUT3), and vascular endothelial growth factor (VEGF). The matricellular protein can be considered a potential therapeutic target, as it can promote tumor growth and confer drug resistance in breast cancer. Numerous tactics, including neutralizing antibodies, antisense oligonucleotides, natural compounds, recombinant proteins, and short hairpin RNAs have been suggested to block its function. This review highlights the structure of CTGF, regulation of its expression, and current knowledge of its oncogenic role in breast cancer, as well as focusing on potential therapeutic strategies for targeting CTGF in breast cancer.
- 13 February 2025
- Published by Springer Nature in Cancer and Metastasis Reviews
- Vol. 44 (1) , 32
CTGF (CCN2): a multifaceted mediator in breast cancer progression and therapeutic targeting
Breast cancer, with its diverse subtypes like ER-positive, HER-2-positive, and triple-negative, presents complex challenges demanding personalized treatment approaches. The intricate interplay of genetic, environmental, and lifestyle factors underscores its status as a primary contributor to cancer-related fatalities in women globally. Understanding the molecular drivers specific to each subtype is crucial for developing effective therapies. In this landscape, connective tissue growth factor (CTGF), also referred to as cellular communication network factor 2 (CCN2), emerges as a significant player. CTGF regulates critical biological activities like cell growth, invasion, and migration, impacting breast cancer development and progression. It modulates breast tumor microenvironment by promoting angiogenesis, activating cancer-associated fibroblasts (CAFs), and inducing inflammation. The activity of CTGF depends on several factors including oxygen levels, hormone signals, and growth factors and differs according to the type of breast cancer. CTGF can regulate breast cancer cells by activating various signaling pathways and modulating the transcription of other genes that are involved in tumor development and metastasis including S100A4, glucose transporter 3 (GLUT3), and vascular endothelial growth factor (VEGF). The matricellular protein can be considered a potential therapeutic target, as it can promote tumor growth and confer drug resistance in breast cancer. Numerous tactics, including neutralizing antibodies, antisense oligonucleotides, natural compounds, recombinant proteins, and short hairpin RNAs have been suggested to block its function. This review highlights the structure of CTGF, regulation of its expression, and current knowledge of its oncogenic role in breast cancer, as well as focusing on potential therapeutic strategies for targeting CTGF in breast cancer.
- 15 May 2024
- Published by Springer Nature
- p. 461-484
Molecular Pathways in Breast Cancer Chemoresistance
- 15 May 2024
- Published by Springer Nature
- p. 461-484
Molecular Pathways in Breast Cancer Chemoresistance
- 18 July 2023
- Published by Springer Nature
- p. 1-24
Molecular Pathways in Breast Cancer Chemoresistance
- 21 June 2023
- Published by Wiley in Biopolymers
- Vol. 114 (9) , e23556
Beyond traditional therapy: Mucoadhesive polymers as a new frontier in oral cancer management
In recent times mucoadhesive drug delivery systems are gaining popularity in oral cancer. It is a malignancy with high global prevalence. Despite significant advances in cancer therapeutics, improving the prognosis of late‐stage oral cancer remains challenging. Targeted therapy using mucoadhesive polymers can improve oral cancer patients' overall outcome by offering enhanced oral mucosa bioavailability, better drug distribution and tissue targeting, and minimizing systemic side effects. Mucoadhesive polymers can also be delivered via different formulations such as tablets, films, patches, gels, and nanoparticles. These polymers can deliver an array of medicines, making them an adaptable drug delivery approach. Drug delivery techniques based on these mucoadhesive polymers are gaining traction and have immense potential as a prospective treatment for late‐stage oral cancer. This review examines leading research in mucoadhesive polymers and discusses their potential applications in treating oral cancer.
- 21 June 2023
- Published by Wiley in Biopolymers
- Vol. 114 (9) , e23556
Beyond traditional therapy: Mucoadhesive polymers as a new frontier in oral cancer management
In recent times mucoadhesive drug delivery systems are gaining popularity in oral cancer. It is a malignancy with high global prevalence. Despite significant advances in cancer therapeutics, improving the prognosis of late‐stage oral cancer remains challenging. Targeted therapy using mucoadhesive polymers can improve oral cancer patients' overall outcome by offering enhanced oral mucosa bioavailability, better drug distribution and tissue targeting, and minimizing systemic side effects. Mucoadhesive polymers can also be delivered via different formulations such as tablets, films, patches, gels, and nanoparticles. These polymers can deliver an array of medicines, making them an adaptable drug delivery approach. Drug delivery techniques based on these mucoadhesive polymers are gaining traction and have immense potential as a prospective treatment for late‐stage oral cancer. This review examines leading research in mucoadhesive polymers and discusses their potential applications in treating oral cancer.
- 5 June 2023
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1869 (7) , 166782
Magnolol and Temozolomide exhibit a synergistic anti-glioma activity through MGMT inhibition
- 5 June 2023
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1869 (7) , 166782
Magnolol and Temozolomide exhibit a synergistic anti-glioma activity through MGMT inhibition
- Open Access
- 1 June 2023
- Published by JCDR Research and Publications in Journal of Clinical and Diagnostic Research
- Vol. 17 (6) , FC1-FC4
Impact of Atorvastatin on C-reactive Protein, Glycaemic Status and Liver Enzymes among Non Diabetic Patients: A Prospective Study
Journal of Clinical and Diagnostic Research aims to publish findings of doctors at grass root level and post graduate students, so that all unique medical experiences are recorded in literature.
- 1 June 2023
- Published by JCDR Research and Publications in Journal of Clinical and Diagnostic Research
- Vol. 17 (6) , FC1-FC4
Open AccessImpact of Atorvastatin on C-reactive Protein, Glycaemic Status and Liver Enzymes among Non Diabetic Patients: A Prospective Study
Journal of Clinical and Diagnostic Research aims to publish findings of doctors at grass root level and post graduate students, so that all unique medical experiences are recorded in literature.
- 1 February 2023
- Published by Elsevier in Experimental Cell Research
- Vol. 424 (1) , 113488
Magnolol induces cytotoxic autophagy in glioma by inhibiting PI3K/AKT/mTOR signaling
- 1 February 2023
- Published by Elsevier in Experimental Cell Research
- Vol. 424 (1) , 113488
Magnolol induces cytotoxic autophagy in glioma by inhibiting PI3K/AKT/mTOR signaling
- 2 February 2022
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Reviews on Cancer
- Vol. 1877 (2) , 188692
Understanding the function and regulation of Sox2 for its therapeutic potential in breast cancer
- 2 February 2022
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Reviews on Cancer
- Vol. 1877 (2) , 188692
Understanding the function and regulation of Sox2 for its therapeutic potential in breast cancer
- 1 April 2021
- Published by Elsevier in Carbohydrate Polymers
- Vol. 258, 117717
Sericin-chitosan-glycosaminoglycans hydrogels incorporated with growth factors for in vitro and in vivo skin repair
- 1 April 2021
- Published by Elsevier in Carbohydrate Polymers
- Vol. 258, 117717
Sericin-chitosan-glycosaminoglycans hydrogels incorporated with growth factors for in vitro and in vivo skin repair