The largest database of trusted experimental protocols
> Disorders > Neoplastic Process > Mantle-Cell Lymphoma

Mantle-Cell Lymphoma

Mantle-Cell Lymphoma: A rare and aggressive type of non-Hodgkin's lymphoma that originates from B-cells in the outer mantle zone of lymphoid follicles.
It is characterized by the overexpression of the cyclin D1 protein, which leads to cell cycle dysregulation and uncontrolled cellular proliferation.
Mantle-Cell Lymphoma often presents with advanced-stage disease and can involve the bone marrow, gastrointestnal tract, and other extranodal sites.
Prompt diagnosis and appropriate treamtent are crucial for managing this challenging malignancy.

Most cited protocols related to «Mantle-Cell Lymphoma»

To demonstrate the performance of the ZIP-based delta scoring, we considered a recent cancer drug screen study involving ibrutinib in combination with 466 compounds for the activated B-cell-like subtype (ABC) of diffuse large B-cell lymphoma (DLBCL) [14] (link). Ibrutinib is a small molecule targeting Bruton's tyrosine kinase (BTK) approved for the treatment of mantle cell lymphoma and chronic lymphocytic leukemia [16] (link). In this study, a high-throughput drug combination screening was used to identify other compounds that can synergistically interact with ibrutinib to improve its anticancer efficacy and circumvent drug resistance. For each drug pair, a 6 × 6 dose–response matrix design was utilized, where the drug effect was measured as percentage of cell viability using TMD8 cancer cell line. The raw combination data was provided by the authors via personal communication, but can now be downloaded from https://tripod.nih.gov/matrix-client/rest/matrix/export/241. We transformed the original percentage viability data into the percentage inhibition data before applying the drug combination analysis to be compatible with the mathematical formulation defined in the Methods section.
We ran the ZIP model on the drug combination data and calculated a summary delta score Δ for each drug pair by taking the average of all the delta scores over its dose combinations, i.e., Δ=1ni=1nδ, where n is the number of dose combinations and n = 25 for a 6 × 6 dose–response matrix (monotherapy responses were removed). We compared the summary delta scores with the other scores derived from the HSA-, Bliss- and Loewe-based models. For HSA and Bliss, there were existing scores implemented in the original study [14] (link), which were based on the following methods: 1) NumExcess is the number of wells in the dose matrix that produced higher effect than both of the individual drug effects; 2) ExcessHSA is the sum of differences between the combination effect and the expected HSA effect; 3) MedianExcess is the median of the HSA excess; 4) ExcessCRX is an extension of the HSA model that was adjusted by dilution factors; 5) LS3 × 3 is the ExcessHSA applied to a 3 × 3 block showing the best HSA synergy in the dose matrix; 6) Beta (β) is the interaction parameter minimizing the deviance from the Bliss independence model over all dose combinations defined as argminβ1ycβ1y11y22 ; and 7) Gamma (γ) is a combination of HSA and Bliss models minimizing argminγ1ycγmax1y1,1y22. For the Loewe-based models, we calculated the two common interaction indices CI (Eq. (8)) and alpha(a) (Eq. (9)). The CI was calculated using an R package SYNERGY [13] (link) and the alpha score was estimated using the R package drc[12] .
Publication 2015
B-Lymphocytes Cell Lines Cell Survival Chronic Lymphocytic Leukemia Diffuse Large B-Cell Lymphoma Drug Combinations Gamma Rays ibrutinib Malignant Neoplasms Mantle-Cell Lymphoma Pharmaceutical Preparations Psychological Inhibition Resistance, Drug Technique, Dilution Tyrosine Kinase, Agammaglobulinaemia

Protocol full text hidden due to copyright restrictions

Open the protocol to access the free full text link

Publication 2020
Chronic Lymphocytic Leukemia Exome Genome Lymphoma Lymphoma, Non-Hodgkin, Familial Mantle-Cell Lymphoma Mutation Reproduction Transcriptome
The AHS is a prospective cohort study of 52,394 licensed private pesticide applicators in Iowa (IA) and North Carolina (NC), 32,346 spouses of these private applicators, and 4,916 licensed commercial applicators from IA. A detailed description of this cohort has been described.(14 (link)) Briefly, applicators were recruited at pesticide licensing stations from December 1993 through December 1997. Private applicators are generally farmers or nursery workers, and commercial applicators are persons employed by pest control companies or businesses that use pesticide applications, such as grain elevators. At enrollment, applicators completed a self-administered questionnaire that provided detailed information on various agricultural exposures, basic demographics, and lifestyle information. Spouses provided such information though a mailed questionnaire sent home with applicators.
We calculated SIRs to compare the cancer experience of licensed private pesticide applicators and their spouses in IA and NC to the general populations in those states. Commercial applicators were only recruited from Iowa and incidence rates were compared to those for the general population of that state. Cohort members were linked to cancer registry files for case identification and to the state death registries and to the National Death Index to ascertain vital status. AHS data release P1REL0712.01 was used, which includes observed numbers of cases for each cancer site that were accrued from the time of enrollment into the AHS (1993–1997) through December 31, 2006; cancer cases identified by the cancer registries as having occurred prior to enrollment were not included. Person-year accumulation began on the date of enrollment in the study and ended on December 31 2006, the last date known alive, the date of cancer diagnosis, or the date the study participant left the state of IA or NC, whichever came first. Cohort members were matched annually to current address records of the Internal Revenue Service, motor vehicle registration offices, and pesticide license registries of state agricultural departments to identify whether the participants continued to reside in Iowa or North Carolina. Less than 1% of the cohort moved out of state (N=390). Expected numbers of cases were calculated by applying 5-year age, calendar year, race and gender-specific incidence rates from IA or NC to the person-year distribution of the cohort using SEER*Stat Version 6.6.1 (http://seer.cancer.gov/seerstat/). Statistical significance of the SIRs was calculated based on Poisson 95% confidence intervals (CIs) as described by Breslow and Day.(15 ) SIRs were reported when there were at least 5 observed cases. Stratified SIRs by smoking status (never, former, current smoker) and state/subject type (private applicators from IA, private applicators from NC, IA spouses, and NC spouses) were also evaluated. Expanded subgroups for non-Hodgkin lymphoma (NHL) were presented to account for the known etiologic heterogeneity among various subtypes.(16 (link)) These subgroups include B-cell subtypes, diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), chronic lymphocytic leukemia/small lymphocytic lymphoma/mantle cell lymphoma (CLL/SLL/MCL), marginal zone lymphoma (MZL), and all T-cell subtypes combined.
Our previous analysis revealed a deficit for all cancers in AHS farmers and spouses.(13 (link)) Consequently, a test of the null hypothesis of one for a cause-specific SIR fails to account for this overall cancer deficit. Therefore, we also evaluated whether there was an excess or deficit of cancer cases for each specific cause relative to the overall deficit of cancers in AHS subjects. To do this, we calculated the ratio of the SIR for each site to the SIR for all cancer sites overall minus that site of interest [i.e., sitex vs. sitenot x]. This approach is related to the comparison of SMRs for exposed and unexposed groups as described in Breslow and Day.(15 ) These relative standardized incidence ratio (RSIR) and 95% CIs are presented for private applicators and spouses. Interpretability of the RSIR is predicated on the assumption that those factors responsible for the observed deficit for all cancers apply across the individual cancer sites in the absence of applicator-related factors.
Publication 2010
B-Lymphocytes Cereals Diagnosis Diffuse Large B-Cell Lymphoma Farmers Genetic Heterogeneity Lymphoid Leukemia Lymphoma, Follicular Lymphoma, Non-Hodgkin, Familial Malignant Neoplasms Mantle-Cell Lymphoma Mucosa-Associated Lymphoid Tissue Lymphoma Pesticides Systemic Inflammatory Response Syndrome T-Lymphocyte Workers
This international open-label, phase 2 study was conducted at 18 sites. Patients with mantle-cell lymphoma were enrolled without randomization and were classified as either having received treatment with bortezomib (≥2 cycles) or not having received such treatment (<2 complete cycles or no prior bortezomib therapy). Single-agent bortezomib is a treatment approved by the Food and Drug Administration for patients with mantle-cell lymphoma that has progressed after at least one initial treatment. Therefore, a defined cohort of patients with prior bortezomib treatment was included in this study, and the combination of the two cohorts was representative of a broad population of patients with relapsed or refractory mantle-cell lymphoma. Patients received single-agent ibrutinib administered orally at a daily dose of 560 mg until progression of disease or until unacceptable levels of adverse events occurred. All the patients provided written informed consent.
The institutional review board at each site approved the study protocol, which was conducted according to the principles of the Declaration of Helsinki and the International Conference on Harmonisation Guidelines for Good Clinical Practice. The protocol, including the statistical analysis plan, is available with the full text of this article at NEJM.org.
Publication 2013
Bortezomib Conferences Disease Progression Ethics Committees, Research ibrutinib Mantle-Cell Lymphoma Patient Representatives Patients
The study panel comprised a total of 117 SMZL samples obtained from frozen spleen biopsies of newly diagnosed, previously untreated patients, and was distinguished into a discovery panel (n = 8 cases), a screening panel (n = 32 cases), and an extension panel (n = 77 cases). Out of the 109 SMZLs used as screening and extension panel, 61 were already reported (Rossi et al., 2011 (link)). In all cases, the SMZL diagnosis was based on spleen histology and was confirmed by centralized pathological revision (S.A. Pileri). Consistent with a SMZL diagnosis, all cases of the discovery and screening panels lacked the t(11;18) and the t(14;18) translocations (Matutes et al., 2008 (link)), and all 117 cases lacked the BRAF p.V600E mutation (Swerdlow et al., 2008 ; Tiacci et al., 2012 (link)). Matched normal DNA was obtained from saliva or peripheral blood granulocytes in 48 patients (n = 8 discovery cases and 40 cases from the screening and extension panel). The clinical and biological characteristics of cases belonging to the SMZL discovery, screening, and extension panels are summarized in Tables S1, S5, and S6, respectively.
For comparative purposes, 399 B cell tumors other than SMZL were also included in the study (18 nodal MZ lymphomas, 65 extranodal MZ lymphomas, 100 chronic lymphocytic leukemias, 20 mantle cell lymphomas, 20 follicular lymphomas, 134 DLBCLs, 20 BRAF p.V600E mutation-positive hairy cell leukemias, and 22 multiple myelomas). All of the 399 samples had been obtained at diagnosis from the involved site (lymph nodes or extranodal sites in the case of lymphoma; CD138+ cells purified from bone marrow aspirates in the case of multiple myeloma; peripheral blood purified B cells in the case of hairy cell leukemia; and peripheral blood mononuclear cells in the case of chronic lymphocytic leukemia). The number of mature B cell neoplasms included in each panel was estimated to allow a 90% probability of identifying genes that are mutated in at least 10% of cases.
Patients provided informed consent in accordance with local IRB requirements and The Declaration of Helsinki. The study was approved by the Ethical Committee of the Ospedale Maggiore della Carità di Novara affiliated with the Amedeo Avogadro University of Eastern Piedmont (Protocol Code 59/CE; Study Number CE 8/11) and by the Institutional Review Board of Columbia University.
Publication 2012
B-Lymphocytes Biopharmaceuticals Biopsy BLOOD Bone Marrow BRAF protein, human Cells Chronic Lymphocytic Leukemia Diagnosis Ethics Committees, Research Freezing Genes, vif Granulocyte Hairy Cell Leukemia Lymphoma Lymphoma, Follicular Mantle-Cell Lymphoma Multiple Myeloma Mutation Neoplasms Nodes, Lymph Patients PBMC Peripheral Blood Mononuclear Cells SDC1 protein, human Sialorrhea Spleen Translocation, Chromosomal

Most recents protocols related to «Mantle-Cell Lymphoma»

Interphase FISH was performed without sorting on 200 cells from 50 cases from PB, BM or LN samples using a commercial probe panel (MetaSystems, Altlussheim, Germany). Panels included TP53/CEP17 (del17p), ATM (del11q), trisomy 12, D13S29 (del13q), and translocations between IGH and the partner gene (IGH/CCND1). The t(11;14)(q13;q12) IGH/CCND1 dual- color dual- fusion translocation probe was used to identify and rule out cases of mantle cell lymphoma (MCL). Cases with del13q alone or absence of FISH aberrations were categorized as a favorable group according to the Dohner FISH classification (11 (link)), while cases with del11q or del17p were considered unfavorable. The group of patients with trisomy 12 was considered to have an intermediate prognosis. The probe cutoff values were set as 5% for the deletion probe, 3% for the trisomy probe, and 1% for the dual-color dual- fusion probe.
Publication 2023
CCND1 protein, human Cells Deletion Mutation Fishes Genes Interphase Mantle-Cell Lymphoma Patients Prognosis TP53 protein, human Translocation, Chromosomal Trisomy
Participant variables included sex (male/female), race (White/Black/others), age at diagnosis (< 60 years/≥ 60 years) (15 (link)), year of diagnosis (2007–2011/2012–2016), marital status (married/unmarried), pathological type (DLBCL/others), surgery (yes/no evidence), radiotherapy (yes/no evidence), and chemotherapy (yes/no evidence) (9 (link)). Other races included American Indian/Alaska Native and Asian/Pacific Islander. Other pathological types included precursor non-Hodgkin B-cell lymphoma; chronic/small lymphocytic leukemia/lymphoma; mantle-cell lymphoma; lymphoplasmacytic lymphoma; intravascular large B-cell lymphoma; Burkitt lymphoma/leukemia; extranodal margin zone lymphoma (MZL); mucosa-associated lymphoid tissue (MALT) cell lymphoma; follicular lymphoma; plasmacytoma; multiple myeloma/plasma-cell leukemia; non-Hodgkin 1ymphoma, B-cell, not otherwise specified (NOS); peripheral T-cell lymphoma, NOS; anaplastic large cell lymphoma, T-/null-cell lymphoma; adult T-cell leukemia/lymphoma; and non-Hodgkin lymphoma, NOS, unknown lineage (12 ).
NCSS was defined as the period from the date of diagnosis to death from non-cancer-specific causes (5 (link)). Follow-up time was calculated as the period from the date of diagnosis with PCNSL until the date of death or last follow-up on December 31, 2016.
Publication 2023
Alaskan Natives American Indians Asian Persons B-Lymphocytes Burkitt Leukemia Burkitt Lymphoma CD30+ Anaplastic Large Cell Lymphoma Cells Chronic Lymphocytic Leukemia Diagnosis Leukemia Leukemia, Plasma Cell Lymphoma Lymphoma, Follicular Lymphoma, Non-Hodgkin, Familial Males Malignant Neoplasms Mantle-Cell Lymphoma Mucosa-Associated Lymphoid Tissue Lymphoma Multiple Myeloma Operative Surgical Procedures Pacific Islander Americans Peripheral T-Cell Lymphoma Pharmacotherapy Plasmacytoma Pre-B Lymphocytes Radiotherapy Reticulosarcoma T-Cell Leukemia-Lymphomas, Adult T-Cell Lymphoma Waldenstrom Macroglobulinemia Woman Zinostatin
We performed a retrospective analysis to evaluate the role of total body irradiation (TBI) in the conditioning regimen of autologous stem cell transplantation (autoSCT) and allogenic stem cell transplantation (alloSCT) in mantle cell lymphoma (MCL). Data were collected from May 2004 until February 2015 at the University Hospital of Muenster, Germany. The multimodal treatment was carried out according to interdisciplinary tumor board recommendation. The patients received total body irradiation in the Department of Radiation Oncology followed by stem cell transplantation at the Department of Hematology and Oncology. TBI was performed with the patient lying down in a bed and rotating in four positions shielded by 2 cm of acrylic glass to ensure adequate surface dosage. The bed is specially modified for TBI and is located at a distance of 545 cm from the focus of the linear accelerator. The total body irradiation was applied after computertomography-based three dimensional (3D) planning with 15 MV photons of a linear accelerator. An accompanying evaluation of dosimetry on patients was performed using diode system with detectors glued to the skin in eight positions (head, larynx, neck, mediastinum, left and right thorax, left and right abdomen) to secure the correct application of radiation dose. A possible adjustment of the monitor units based on the measured values is agreed between treating physician and medical physicist. TBI with a total dose of more than 8 Gy was performed with individual lung shielding to ensure effective protection against acute or chronic side effects. If patients were treated with lung shielding, they received individually adapted radiation of mediastinal and axillary lymph nodes as compensation. For mediastinal and axillary radiotherapy, 3D-conformal radiotherapy (3D-CRT) with 6 and 15 MV photons was applied. Daily online imaging verifications are performed before each radiation fraction for precise positioning control of patients. Total body irradiation, high-dose chemotherapy and stem cell transplantation are performed under inpatient treatment at the Bone Marrow Transplantation Unit, University Hospital of Muenster.
Publication 2023
Abdomen Acclimatization Axilla Bone Marrow Transplantation Chest Combined Modality Therapy Head Hospitalization Larynx Linear Accelerators Lung Mantle-Cell Lymphoma Mediastinum Neck Neoplasms Nodes, Lymph Patients Pharmacotherapy Physicians Positioning, Patient Radiometry Radiotherapy, Conformal Skin Transplantation, Hematopoietic Stem Cell Treatment Protocols Whole-Body Irradiation
The archives of the Department of Hematopathology at The University of Texas MD Anderson Cancer Center were searched for high-grade B-cell lymphomas with blastoid morphology diagnosed between 1 January 2012 and 31 December 2021. We applied the inclusion and exclusion criteria described previously with modifications [4 (link)]. Briefly, inclusion criteria included HGBL cases with blastoid morphology involving any tissue site. Blastoid morphology in this study was defined as medium-size lymphoma cells with a scant amount of cytoplasm, finely dispersed nuclear chromatin, and inconspicuous nucleoli or small distinct nucleoli, if present, resembling lymphoblasts in hematoxylin and eosin-stained tissue sections, touch preparations, or aspirate smears if available [6 (link)]. Blastoid morphology was reviewed and confirmed by at least two pathologists independently in a blinded manner. The exclusion criteria were: (1) patients with a diagnosis of Burkitt lymphoma, B-ALL, blastoid variant of mantle cell lymphoma (including cyclin D1-negative cases), and blastoid follicular lymphoma; (2) cases with processing artifact that precluded adequate morphologic assessment; (3) cases in which MYC rearrangement status was not available. Forty-seven cases of B-ALL, diagnosed during the same time interval, were included as a comparison group. The diagnosis of blastoid HGBL and B-ALL was made according to the criteria defined in the 4th WHO Classification [6 (link)] and, for cases difficult to classify based on WHO criteria, the diagnosis was further confirmed by the gene transcriptome profile. For the purpose of this study, a disproportionally large subset of CD34-negative B-ALL (n = 25) cases were included. For the purpose of the study, previously reported cases were included [4 (link),5 (link)]. The corresponding medical records were reviewed to obtain clinical information.
Publication 2023
B-Cell Lymphomas Burkitt Leukemia Burkitt Lymphoma Cell Nucleolus Chromatin Cyclin D1 Cytoplasm Diagnosis Eosin Genes Hematoxylin Lymphoma Lymphoma, Follicular Malignant Neoplasms Mantle-Cell Lymphoma Pathologists Patients Tissues Tissue Stains Touch
The registry prospectively records the gender, age, ethnic group, smoking status, age at diagnosis of IBD, type of IBD, location of disease, need for admission or surgery, treatments for IBD including immunomodulator and biological treatments with dates of start and withdrawal of each of these drugs and date of last evaluation. Additional information about lymphomas provided by the investigators of each participating center includes type of lymphoma, date of diagnosis, stage following the Lugano classification [7 (link)], clinical presentation, diagnostic test, treatment, relapse, and consensus about the management with hematology. These additional data were collected and managed using REDCap electronic data capture tools hosted at the Asociación Española de Gastroenterología (AEG; www.aegastro.es; accessed on 1 June 2022) [8 (link),9 (link)]. We defined two NHL subtypes by rate of progression (aggressive and indolent) following the World Health Organization’s (WHO) classification [6 (link)]. Diffuse large B-cell lymphoma, mantle cell lymphoma, plasmablastic lymphoma, and cutaneous lymphoma were defined as aggressive NHL. Indolent NHL included follicular, marginal zone, and lymphoplasmacytic lymphoma.
Publication 2023
Biopharmaceuticals Diagnosis Diffuse Large B-Cell Lymphoma Disease Progression Ethnicity Gender Immunoblastic Large-Cell Lymphoma Immunologic Adjuvants Lymphoma Mantle-Cell Lymphoma Operative Surgical Procedures Pharmaceutical Preparations Relapse Skin Tests, Diagnostic Waldenstrom Macroglobulinemia

Top products related to «Mantle-Cell Lymphoma»

Sourced in United States, China, United Kingdom, Germany, Australia, Japan, Canada, Italy, France, Switzerland, New Zealand, Brazil, Belgium, India, Spain, Israel, Austria, Poland, Ireland, Sweden, Macao, Netherlands, Denmark, Cameroon, Singapore, Portugal, Argentina, Holy See (Vatican City State), Morocco, Uruguay, Mexico, Thailand, Sao Tome and Principe, Hungary, Panama, Hong Kong, Norway, United Arab Emirates, Czechia, Russian Federation, Chile, Moldova, Republic of, Gabon, Palestine, State of, Saudi Arabia, Senegal
Fetal Bovine Serum (FBS) is a cell culture supplement derived from the blood of bovine fetuses. FBS provides a source of proteins, growth factors, and other components that support the growth and maintenance of various cell types in in vitro cell culture applications.
Sourced in United States, Germany, China
The Jeko-1 is a cell line derived from a patient with mantle cell lymphoma. It is a suspension cell line and can be used for research purposes related to this type of lymphoma.
Sourced in United States, China, Germany, United Kingdom, Japan, France, Canada, Australia, Italy, Switzerland, Belgium, New Zealand, Spain, Israel, Sweden, Denmark, Macao, Brazil, Ireland, India, Austria, Netherlands, Holy See (Vatican City State), Poland, Norway, Cameroon, Hong Kong, Morocco, Singapore, Thailand, Argentina, Taiwan, Province of China, Palestine, State of, Finland, Colombia, United Arab Emirates
RPMI 1640 medium is a commonly used cell culture medium developed at Roswell Park Memorial Institute. It is a balanced salt solution that provides essential nutrients, vitamins, and amino acids to support the growth and maintenance of a variety of cell types in vitro.
Sourced in United States, China, United Kingdom, Germany, France, Canada, Japan, Australia, Italy, Switzerland, Belgium, New Zealand, Austria, Netherlands, Israel, Sweden, Denmark, India, Ireland, Spain, Brazil, Norway, Argentina, Macao, Poland, Holy See (Vatican City State), Mexico, Hong Kong, Portugal, Cameroon
RPMI 1640 is a common cell culture medium used for the in vitro cultivation of a variety of cells, including human and animal cells. It provides a balanced salt solution and a source of essential nutrients and growth factors to support cell growth and proliferation.
Sourced in Germany
Granta-519 is a high-quality microbiological incubator produced by Granta Instruments. The incubator is designed for precise temperature control and uniform air circulation to ensure optimal growth conditions for a variety of microbial cultures. The device features a robust construction and user-friendly controls for efficient operation.
Sourced in United States, Germany
The Z-138 is a versatile laboratory centrifuge designed for a variety of applications. It features a compact and durable construction, enabling efficient separation and concentration of samples. The centrifuge can accommodate multiple rotor types and sample volumes, making it suitable for diverse research and diagnostic needs.
Sourced in United States, Germany, United Kingdom, China, Canada, France, Japan, Australia, Switzerland, Israel, Italy, Belgium, Austria, Spain, Gabon, Ireland, New Zealand, Sweden, Netherlands, Denmark, Brazil, Macao, India, Singapore, Poland, Argentina, Cameroon, Uruguay, Morocco, Panama, Colombia, Holy See (Vatican City State), Hungary, Norway, Portugal, Mexico, Thailand, Palestine, State of, Finland, Moldova, Republic of, Jamaica, Czechia
Penicillin/streptomycin is a commonly used antibiotic solution for cell culture applications. It contains a combination of penicillin and streptomycin, which are broad-spectrum antibiotics that inhibit the growth of both Gram-positive and Gram-negative bacteria.
Sourced in United States, United Kingdom, Germany, China, France, Canada, Australia, Japan, Switzerland, Italy, Belgium, Israel, Austria, Spain, Netherlands, Poland, Brazil, Denmark, Argentina, Sweden, New Zealand, Ireland, India, Gabon, Macao, Portugal, Czechia, Singapore, Norway, Thailand, Uruguay, Moldova, Republic of, Finland, Panama
Streptomycin is a broad-spectrum antibiotic used in laboratory settings. It functions as a protein synthesis inhibitor, targeting the 30S subunit of bacterial ribosomes, which plays a crucial role in the translation of genetic information into proteins. Streptomycin is commonly used in microbiological research and applications that require selective inhibition of bacterial growth.
Sourced in United States, Germany, United Kingdom, Japan, Italy, China, Macao, Switzerland, France, Canada, Sao Tome and Principe, Spain, Australia, Ireland, Poland, Belgium, Denmark, India, Sweden, Israel, Austria, Brazil, Czechia, Netherlands, Portugal, Norway, Holy See (Vatican City State), New Zealand, Hungary, Senegal, Argentina, Thailand, Singapore, Ukraine, Mexico
FBS, or Fetal Bovine Serum, is a commonly used cell culture supplement. It is derived from the blood of bovine fetuses and provides essential growth factors, hormones, and other nutrients to support the growth and proliferation of a wide range of cell types in vitro.
Sourced in United States, Germany, China
The Rec-1 is a laboratory equipment designed for the recovery and concentration of microorganisms from various sample types. It utilizes a filtration-based process to separate and retain target microorganisms, which can then be further analyzed or cultured.

More about "Mantle-Cell Lymphoma"

Mantle Cell Lymphoma (MCL) is a rare and aggressive subtype of non-Hodgkin's lymphoma that originates from B-cells in the outer mantle zone of lymphoid follicles.
This challenging malignancy is characterized by the overexpression of the cyclin D1 protein, leading to cell cycle dysregulation and uncontrolled cellular proliferation.
MCL often presents with advanced-stage disease and can involve the bone marrow, gastrointestinal tract, and other extranodal sites.
Prompt diagnosis and appropriate treatment are crucial for managing this condition.
Key cell lines used in MCL research include FBS, Jeko-1, Granta-519, Z-138, and Rec-1, which are typically cultured in RPMI 1640 medium supplemented with penicillin/streptomycin.
Understanding the molecular mechanisms and signaling pathways underlying MCL is essential for developing more effective therapies.
By leveraging AI-driven platforms like PubCompare.ai, researchers can optimize their MCL studies, enhance reproducibility, and make informed decisions to advance this field of research.