leptin and Hematologic-Neoplasms

leptin has been researched along with Hematologic-Neoplasms* in 5 studies

Reviews

1 review(s) available for leptin and Hematologic-Neoplasms

ArticleYear
Role of leptin and leptin receptors in hematological malignancies.
    Leukemia & lymphoma, 2016, Volume: 57, Issue:1

    Leptin is an adipose-derived cytokine that has an important role in bodyweight homeostasis and energy balance. There are a number of studies which have suggested that leptin and its receptors dysregulation play a critical role in the development of malignancies including hematological malignancies, mainly via activation of the JAK/STAT pathway which regulates downstream signaling pathways such as PI3K/AKT signaling and ERK1/2. In this review, current understandings of leptin/leptin receptors mediated pathogenesis in various lymphoid malignancies are described. Blocking of the leptin receptor might be a unique therapeutic approach for many hematological malignancies.

    Topics: Animals; Gene Expression Regulation; Hematologic Neoplasms; Humans; Leptin; Polymorphism, Genetic; Protein Binding; Receptors, Leptin; Risk; Signal Transduction

2016

Other Studies

4 other study(ies) available for leptin and Hematologic-Neoplasms

ArticleYear
Leptin and resistin levels in serum of patients with hematologic malignancies: correlation with clinical characteristics.
    Experimental oncology, 2006, Volume: 28, Issue:3

    To evaluate leptin and resistin levels in patients with various hematologic malignancies.. We included 21 patients with lymphoma, 14 with multiple myeloma (MM), 14 with acute leukemia, 13 with chronic lymphocytic leukemia (CLL), and 25 healthy control subjects into our study. The subjects' body mass indexes (BMI) were calculated; hematological and acute phase response parameters, serum lipid were determined; serum leptin and resistin levels were determined by ELISA.. Serum leptin level was significantly increased in CLL and MM groups when compared to the control group (p less, similar 0.01). Resistin level was significantly higher in lymphoma patients than in CLL, acute leukemia and control groups (p less, similar 0.01). In the control group, leptin level was negatively correlated with hemoglobin level (r = -0.44, p = 0.047); and in all patients with hematologic malignancies, leptin level was correlated with BMI (r = 0.32, p = 0.02). Leptin in lymphoma subjects correlated with hemoglobin level (r = 0.64, p = 0.005), resistin level correlated with the platelet count in patients with hematologic malignancies (r = 0.26, p = 0.044). In addition, leptin level had negative correlations with international prognostic score (IPS) in Hodgkin lymphoma (r = -0.9, p = 0.002) and with international prognostic index (IPI) in non-Hodgkin lymphoma (r = -0.77, p = 0.03). In CLL patients, leptin level had a correlation with the poor prognostic marker - CD38 level (r = 0.68, p = 0.03).. We found higher leptin levels in MM and CLL patients, and higher resistin levels in lymphoma patients: this fact demonstrates that changes in adipose tissue and metabolism occur in these disease states.

    Topics: Adipose Tissue; Adult; Aged; Female; Hematologic Neoplasms; Humans; Leptin; Lipid Metabolism; Male; Middle Aged; Resistin

2006
Plasma leptin levels vary with the periods during chemotherapy.
    American journal of hematology, 2003, Volume: 74, Issue:2

    Topics: Adult; Antineoplastic Agents; Female; Hematologic Neoplasms; Humans; Leptin; Male; Middle Aged; Osmolar Concentration

2003
Bone marrow and peripheral blood leptin levels in lymphoproliferative diseases--relation to the bone marrow fat and infiltration.
    Neoplasma, 2000, Volume: 47, Issue:5

    Leptin is a nonglycosylated protein produced mostly by adipocytes. The role ofleptin in body weight regulation through its anorectic effect in hypothalamus is very well known. Less known are other leptin effects such as the stimulation of hematopoesis and some parts of immunity system. The role of leptin in the pathogenesis of some malignant tumors is discussed. Only a little is known about bone marrow adipocyte leptin production. We examined leptin concentrations in the sera from peripheral blood and bone marrow, the percentage of bone marrow fat, the degree of bone marrow infiltration, the body mass index (BMI) in 42 patients with lymphoproliferative diseases. We found that bone marrow has significantly lower leptin levels (6,6+/-10,9 ng/ml) than peripheral blood (9,1+/-11,5 ng/ml) (p < 0.0001). Bone marrow and peripheral blood leptin levels have also a significant thin correlation (r = +0.91, p < 0.0001). Bone marrow (r = +0.55, p < 0.0005) and peripheral blood (r = +0.52, p < 0.0005) leptin concentrations are significantly correlated to BMI. Blood serum leptin (r = +0.46, p < 0.003) and bone marrow leptin (r = +0.40, p < 0.01) are related to the bone marrow fat percentage. In addition we found a negative correlation of blood serum leptin (r = -0.59, p < 0.0001) and bone marrow leptin (r = -0.42, p < 0.005) to bone marrow malignant infiltration. When we divided the patients into groups with bone marrow infiltration more than 10% and without or less than 10% infiltration, the first group had significantly lower peripheral blood (p < 0.001) and bone marrow (p < 0.02) leptin. We also confirmed a relation of bone marrow fat and infiltration (r = +0.49, p < 0.001). Our results suggest a relationship among leptin levels in blood or bone marrow and bone marrow infiltration in lymphoproliferative diseases. This fact needs further investigation and an evaluation of its application in clinical practice.

    Topics: Adipose Tissue; Biomarkers; Body Mass Index; Bone Marrow; Erythrocyte Count; Female; Hematologic Neoplasms; Hemoglobins; Humans; Leptin; Leukocyte Count; Lymphoproliferative Disorders; Male; Middle Aged; Platelet Count

2000
Serum leptin levels during cancer chemotherapy.
    Annals of hematology, 1998, Volume: 77, Issue:4

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Female; Hematologic Neoplasms; Humans; Leptin; Male; Middle Aged; Obesity; Proteins

1998