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  1. Article ; Online: Unveiling the Protective Role of Melatonin in Osteosarcoma: Current Knowledge and Limitations.

    Al-Ansari, Nojoud / Samuel, Samson Mathews / Büsselberg, Dietrich

    Biomolecules

    2024  Volume 14, Issue 2

    Abstract: Melatonin, an endogenous neurohormone produced by the pineal gland, has received increased interest due to its potential anti-cancer properties. Apart from its well-known role in the sleep-wake cycle, extensive scientific evidence has shown its role in ... ...

    Abstract Melatonin, an endogenous neurohormone produced by the pineal gland, has received increased interest due to its potential anti-cancer properties. Apart from its well-known role in the sleep-wake cycle, extensive scientific evidence has shown its role in various physiological and pathological processes, such as inflammation. Additionally, melatonin has demonstrated promising potential as an anti-cancer agent as its function includes inhibition of tumorigenesis, induction of apoptosis, and regulation of anti-tumor immune response. Although a precise pathophysiological mechanism is yet to be established, several pathways related to the regulation of cell cycle progression, DNA repair mechanisms, and antioxidant activity have been implicated in the anti-neoplastic potential of melatonin. In the current manuscript, we focus on the potential anti-cancer properties of melatonin and its use in treating and managing pediatric osteosarcoma. This aggressive bone tumor primarily affects children and adolescents and is treated mainly by surgical and radio-oncological interventions, which has improved survival rates among affected individuals. Significant disadvantages to these interventions include disease recurrence, therapy-related toxicity, and severe/debilitating side effects that the patients have to endure, significantly affecting their quality of life. Melatonin has therapeutic effects when used for treating osteosarcoma, attributed to its ability to halt cancer cell proliferation and trigger apoptotic cell death, thereby enhancing chemotherapeutic efficacy. Furthermore, the antioxidative function of melatonin alleviates harmful side effects of chemotherapy-induced oxidative damage, aiding in decreasing therapeutic toxicities. The review concisely explains the many mechanisms by which melatonin targets osteosarcoma, as evidenced by significant results from several in vitro and animal models. Nevertheless, if further explored, human trials remain a challenge that could shed light and support its utility as an adjunctive therapeutic modality for treating osteosarcoma.
    MeSH term(s) Animals ; Adolescent ; Child ; Humans ; Melatonin/pharmacology ; Melatonin/therapeutic use ; Melatonin/metabolism ; Quality of Life ; Osteosarcoma/drug therapy ; Antioxidants/pharmacology ; Antioxidants/therapeutic use ; Bone Neoplasms/drug therapy
    Chemical Substances Melatonin (JL5DK93RCL) ; Antioxidants
    Language English
    Publishing date 2024-01-24
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom14020145
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Influence of Gut Microbial Species on Diabetes Mellitus.

    Al-Ishaq, Raghad Khalid / Samuel, Samson Mathews / Büsselberg, Dietrich

    International journal of molecular sciences

    2023  Volume 24, Issue 9

    Abstract: Diabetes mellitus (DM) is a metabolic disorder with an alarming incidence rate and a considerable burden on the patient's life and health care providers. An increase in blood glucose level and insulin resistance characterizes it. Internal and external ... ...

    Abstract Diabetes mellitus (DM) is a metabolic disorder with an alarming incidence rate and a considerable burden on the patient's life and health care providers. An increase in blood glucose level and insulin resistance characterizes it. Internal and external factors such as urbanization, obesity, and genetic mutations could increase the risk of DM. Microbes in the gut influence overall health through immunity and nutrition. Recently, more studies have been conducted to evaluate and estimate the role of the gut microbiome in diabetes development, progression, and management. This review summarizes the current knowledge addressing three main bacterial species:
    MeSH term(s) Humans ; Blood Glucose ; Gastrointestinal Microbiome/physiology ; Diabetes Mellitus ; Hypoglycemic Agents ; Metformin
    Chemical Substances Blood Glucose ; Hypoglycemic Agents ; Metformin (9100L32L2N)
    Language English
    Publishing date 2023-05-01
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms24098118
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The Juggernaut of Adaptive Metabolism in Cancers: Implications and Therapeutic Targets.

    Samuel, Samson Mathews / Kubatka, Peter / Shakibaei, Mehdi / Büsselberg, Dietrich

    Cancers

    2022  Volume 14, Issue 21

    Abstract: The disease of cancer instills a sense of fear and dread among patients and the next of kin who are indirectly affected by the deteriorating quality of life of their loved ones [ ... ]. ...

    Abstract The disease of cancer instills a sense of fear and dread among patients and the next of kin who are indirectly affected by the deteriorating quality of life of their loved ones [...].
    Language English
    Publishing date 2022-10-23
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14215202
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Treating Cancers Using Nature's Medicine: Significance and Challenges.

    Samuel, Samson Mathews / Kubatka, Peter / Büsselberg, Dietrich

    Biomolecules

    2021  Volume 11, Issue 11

    Abstract: There was a time when plant-derived natural formulations were the cornerstone of ancient therapeutic approaches for treating many illnesses [ ... ]. ...

    Abstract There was a time when plant-derived natural formulations were the cornerstone of ancient therapeutic approaches for treating many illnesses [...].
    MeSH term(s) Neoplasms
    Language English
    Publishing date 2021-11-15
    Publishing country Switzerland
    Document type Editorial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom11111698
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Paclitaxel and its semi-synthetic derivatives: comprehensive insights into chemical structure, mechanisms of action, and anticancer properties.

    Sati, Priyanka / Sharma, Eshita / Dhyani, Praveen / Attri, Dharam Chand / Rana, Rohit / Kiyekbayeva, Lashyn / Büsselberg, Dietrich / Samuel, Samson Mathews / Sharifi-Rad, Javad

    European journal of medical research

    2024  Volume 29, Issue 1, Page(s) 90

    Abstract: Cancer is a disease that can cause abnormal cell growth and can spread throughout the body. It is among the most significant causes of death worldwide, resulting in approx. 10 million deaths annually. Many synthetic anticancer drugs are available, but ... ...

    Abstract Cancer is a disease that can cause abnormal cell growth and can spread throughout the body. It is among the most significant causes of death worldwide, resulting in approx. 10 million deaths annually. Many synthetic anticancer drugs are available, but they often come with side effects and can interact negatively with other medications. Additionally, many chemotherapy drugs used for cancer treatment can develop resistance and harm normal cells, leading to dose-limiting side effects. As a result, finding effective cancer treatments and developing new drugs remains a significant challenge. However, plants are a potent source of natural products with the potential for cancer treatment. These biologically active compounds may be the basis for enhanced or less toxic derivatives. Herbal medicines/phytomedicines, or plant-based drugs, are becoming more popular in treating complicated diseases like cancer due to their effectiveness and are a particularly attractive option due to their affordability, availability, and lack of serious side effects. They have broad applicability and therapeutic efficacy, which has spurred scientific research into their potential as anticancer agents. This review focuses on Paclitaxel (PTX), a plant-based drug derived from Taxus sp., and its ability to treat specific tumors. PTX and its derivatives are effective against various cancer cell lines. Researchers can use this detailed information to develop effective and affordable treatments for cancer.
    MeSH term(s) Humans ; Paclitaxel/pharmacology ; Paclitaxel/chemistry ; Antineoplastic Agents/pharmacology ; Antineoplastic Agents/therapeutic use ; Neoplasms/drug therapy ; Plants
    Chemical Substances Paclitaxel (P88XT4IS4D) ; Antineoplastic Agents
    Language English
    Publishing date 2024-01-30
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1329381-3
    ISSN 2047-783X ; 0949-2321
    ISSN (online) 2047-783X
    ISSN 0949-2321
    DOI 10.1186/s40001-024-01657-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: COVID-19 Vaccines and Hyperglycemia-Is There a Need for Postvaccination Surveillance?

    Samuel, Samson Mathews / Varghese, Elizabeth / Triggle, Chris R / Büsselberg, Dietrich

    Vaccines

    2022  Volume 10, Issue 3

    Abstract: The COVID-19 vaccines currently in use have undoubtedly played the most significant role in combating the SARS-CoV-2 virus and reducing disease severity and the risk of death among those affected, especially among those with pre-existing conditions, such ...

    Abstract The COVID-19 vaccines currently in use have undoubtedly played the most significant role in combating the SARS-CoV-2 virus and reducing disease severity and the risk of death among those affected, especially among those with pre-existing conditions, such as diabetes. The management of blood glucose levels has become critical in the context of the COVID-19 pandemic, where data show two- to threefold higher intensive care hospital admissions and more than twice the mortality rate among diabetic COVID-19 patients when compared with their nondiabetic counterparts. Furthermore, new-onset diabetes and severe hyperglycemia-related complications, such as hyperosmolar hyperglycemic syndrome (HHS) and diabetic ketoacidosis (DKA), were reported in COVID-19 patients. However, irrespective of the kind of vaccine and dosage number, possible vaccination-induced hyperglycemia and associated complications were reported among vaccinated individuals. The current article summarizes the available case reports on COVID-19 vaccination-induced hyperglycemia, the possible molecular mechanism responsible for this phenomenon, and the outstanding questions that need to be addressed and discusses the need to identify at-risk individuals and promote postvaccination monitoring/surveillance among at-risk individuals.
    Language English
    Publishing date 2022-03-16
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2703319-3
    ISSN 2076-393X
    ISSN 2076-393X
    DOI 10.3390/vaccines10030454
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: COVID-19 Vaccines and Hyperglycemia—Is There a Need for Postvaccination Surveillance?

    Samson Mathews Samuel / Elizabeth Varghese / Chris R. Triggle / Dietrich Büsselberg

    Vaccines, Vol 10, Iss 454, p

    2022  Volume 454

    Abstract: The COVID-19 vaccines currently in use have undoubtedly played the most significant role in combating the SARS-CoV-2 virus and reducing disease severity and the risk of death among those affected, especially among those with pre-existing conditions, such ...

    Abstract The COVID-19 vaccines currently in use have undoubtedly played the most significant role in combating the SARS-CoV-2 virus and reducing disease severity and the risk of death among those affected, especially among those with pre-existing conditions, such as diabetes. The management of blood glucose levels has become critical in the context of the COVID-19 pandemic, where data show two- to threefold higher intensive care hospital admissions and more than twice the mortality rate among diabetic COVID-19 patients when compared with their nondiabetic counterparts. Furthermore, new-onset diabetes and severe hyperglycemia-related complications, such as hyperosmolar hyperglycemic syndrome (HHS) and diabetic ketoacidosis (DKA), were reported in COVID-19 patients. However, irrespective of the kind of vaccine and dosage number, possible vaccination-induced hyperglycemia and associated complications were reported among vaccinated individuals. The current article summarizes the available case reports on COVID-19 vaccination-induced hyperglycemia, the possible molecular mechanism responsible for this phenomenon, and the outstanding questions that need to be addressed and discusses the need to identify at-risk individuals and promote postvaccination monitoring/surveillance among at-risk individuals.
    Keywords COVID-19 ; diabetes ; diabetic ketoacidosis ; hyperglycemia ; hyperosmolar hyperglycemic syndrome ; SARS-CoV-2 ; Medicine ; R
    Subject code 610
    Language English
    Publishing date 2022-03-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Curcumin, calebin A and chemosensitization: How are they linked to colorectal cancer?

    Brockmueller, Aranka / Samuel, Samson Mathews / Mazurakova, Alena / Büsselberg, Dietrich / Kubatka, Peter / Shakibaei, Mehdi

    Life sciences

    2023  Volume 318, Page(s) 121504

    Abstract: Colorectal cancer (CRC) is one of the leading malignant diseases worldwide with a high rate of metastasis and poor prognosis. Treatment options include surgery, which is usually followed by chemotherapy in advanced CRC. With treatment, cancer cells could ...

    Abstract Colorectal cancer (CRC) is one of the leading malignant diseases worldwide with a high rate of metastasis and poor prognosis. Treatment options include surgery, which is usually followed by chemotherapy in advanced CRC. With treatment, cancer cells could become resistant to classical cytostatic drugs such as 5-fluorouracil (5-FU), oxaliplatin, cisplatin, and irinotecan, resulting in chemotherapeutic failure. For this reason, there is a high demand for health-preserving re-sensitization mechanisms including the complementary use of natural plant compounds. Calebin A and curcumin, two polyphenolic turmeric ingredients derived from the Asian Curcuma longa plant, demonstrate versatile anti-inflammatory and cancer-reducing abilities, including CRC-combating capacity. After an insight into their epigenetics-modifying holistic health-promoting effects, this review compares functional anti-CRC mechanisms of multi-targeting turmeric-derived compounds with mono-target classical chemotherapeutic agents. Furthermore, the reversal of resistance to chemotherapeutic drugs was presented by focusing on calebin A's and curcumin's capabilities to chemosensitize or re-sensitize CRC cells to 5-FU, oxaliplatin, cisplatin, and irinotecan. Both polyphenols enhance the receptiveness of CRC cells to standard cytostatic drugs converting them from chemoresistant into non-chemoresistant CRC cells by modulating inflammation, proliferation, cell cycle, cancer stem cells, and apoptotic signaling. Therefore, calebin A and curcumin can be tested for their ability to overcome cancer chemoresistance in preclinical and clinical trials. The future perspective of involving turmeric-ingredients curcumin or calebin A as an additive treatment to chemotherapy for patients with advanced metastasized CRC is explained.
    MeSH term(s) Humans ; Curcumin/pharmacology ; Irinotecan/pharmacology ; Oxaliplatin/pharmacology ; Cisplatin/pharmacology ; Cytostatic Agents/pharmacology ; Cytostatic Agents/therapeutic use ; Cell Line, Tumor ; Fluorouracil/pharmacology ; Colorectal Neoplasms/pathology ; Drug Resistance, Neoplasm
    Chemical Substances Curcumin (IT942ZTH98) ; Irinotecan (7673326042) ; Oxaliplatin (04ZR38536J) ; Cisplatin (Q20Q21Q62J) ; Cytostatic Agents ; Fluorouracil (U3P01618RT)
    Language English
    Publishing date 2023-02-20
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 3378-9
    ISSN 1879-0631 ; 0024-3205
    ISSN (online) 1879-0631
    ISSN 0024-3205
    DOI 10.1016/j.lfs.2023.121504
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: B7-H3 at the crossroads between tumor plasticity and colorectal cancer progression: a potential target for therapeutic intervention.

    Varghese, Elizabeth / Samuel, Samson Mathews / Brockmueller, Aranka / Shakibaei, Mehdi / Kubatka, Peter / Büsselberg, Dietrich

    Cancer metastasis reviews

    2023  Volume 43, Issue 1, Page(s) 115–133

    Abstract: B7-H3 (B7 homology 3 protein) is an important transmembrane immunoregulatory protein expressed in immune cells, antigen-presenting cells, and tumor cells. Studies reveal a multifaceted role of B7-H3 in tumor progression by modulating various cancer ... ...

    Abstract B7-H3 (B7 homology 3 protein) is an important transmembrane immunoregulatory protein expressed in immune cells, antigen-presenting cells, and tumor cells. Studies reveal a multifaceted role of B7-H3 in tumor progression by modulating various cancer hallmarks involving angiogenesis, immune evasion, and tumor microenvironment, and it is also a promising candidate for cancer immunotherapy. In colorectal cancer (CRC), B7-H3 has been associated with various aspects of disease progression, such as evasion of tumor immune surveillance, tumor-node metastasis, and poor prognosis. Strategies to block or interfere with B7-H3 in its immunological and non-immunological functions are under investigation. In this study, we explore the role of B7-H3 in tumor plasticity, emphasizing tumor glucose metabolism, angiogenesis, epithelial-mesenchymal transition, cancer stem cells, apoptosis, and changing immune signatures in the tumor immune landscape. We discuss how B7-H3-induced tumor plasticity contributes to immune evasion, metastasis, and therapy resistance. Furthermore, we delve into the most recent advancements in targeting B7-H3-based tumor immunotherapy as a potential approach to CRC treatment.
    MeSH term(s) Humans ; B7 Antigens/metabolism ; Colorectal Neoplasms/pathology ; Immunotherapy ; Tumor Microenvironment
    Chemical Substances B7 Antigens ; CD276 protein, human
    Language English
    Publishing date 2023-09-28
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 604857-2
    ISSN 1573-7233 ; 0167-7659
    ISSN (online) 1573-7233
    ISSN 0167-7659
    DOI 10.1007/s10555-023-10137-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Metabolic heterogeneity in TNBCs: A potential determinant of therapeutic efficacy of 2-deoxyglucose and metformin combinatory therapy.

    Samuel, Samson Mathews / Varghese, Elizabeth / Satheesh, Noothan Jyothi / Triggle, Chris R / Büsselberg, Dietrich

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2023  Volume 164, Page(s) 114911

    Abstract: Breast cancers (BCs) remain the leading cause of cancer-related deaths among women worldwide. Among the different types of BCs, treating the highly aggressive, invasive, and metastatic triple-negative BCs (TNBCs) that do not respond to hormonal/human ... ...

    Abstract Breast cancers (BCs) remain the leading cause of cancer-related deaths among women worldwide. Among the different types of BCs, treating the highly aggressive, invasive, and metastatic triple-negative BCs (TNBCs) that do not respond to hormonal/human epidermal growth factor receptor 2 (HER2) targeted interventions since they lack ER/PR/HER2 receptors remains challenging. While almost all BCs depend on glucose metabolism for their proliferation and survival, studies indicate that TNBCs are highly dependent on glucose metabolism compared to non-TNBC malignancies. Hence, limiting/inhibiting glucose metabolism in TNBCs should curb cell proliferation and tumor growth. Previous reports, including ours, have shown the efficacy of metformin, the most widely prescribed antidiabetic drug, in reducing cell proliferation and growth in MDA-MB-231 and MDA-MB-468 TNBC cells. In the current study, we investigated and compared the anticancer effects of either metformin (2 mM) in glucose-starved or 2-deoxyglucose (10 mM; glycolytic inhibitor; 2DG) exposed MDA-MB-231 and MDA-MB-468 TNBC cells. Assays for cell proliferation, rate of glycolysis, cell viability, and cell-cycle analysis were performed. The status of proteins of the mTOR pathway was assessed by Western blot analysis. Metformin treatment in glucose-starved and 2DG (10 mM) exposed TNBC cells inhibited the mTOR pathway compared to non-treated glucose-starved cells or 2DG/metformin alone treated controls. Cell proliferation is also significantly reduced under these combination treatment conditions. The results indicate that combining a glycolytic inhibitor and metformin could prove an efficient therapeutic approach for treating TNBCs, albeit the efficacy of the combination treatment may depend on metabolic heterogeneity across various subtypes of TNBCs.
    MeSH term(s) Female ; Humans ; Metformin/pharmacology ; Metformin/therapeutic use ; Deoxyglucose/pharmacology ; Triple Negative Breast Neoplasms/pathology ; Cell Line, Tumor ; Cell Proliferation ; TOR Serine-Threonine Kinases ; Glucose/metabolism
    Chemical Substances Metformin (9100L32L2N) ; Deoxyglucose (9G2MP84A8W) ; TOR Serine-Threonine Kinases (EC 2.7.11.1) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2023-05-22
    Publishing country France
    Document type Journal Article
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2023.114911
    Database MEDical Literature Analysis and Retrieval System OnLINE

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