keyword
https://read.qxmd.com/read/38503524/-clinical-significance-of-monitoring-nup98-nsd1-fusion-genes-before-and-after-allogeneic-hematopoietic-stem-cell-transplantation
#21
JOURNAL ARTICLE
Y K Shang, X A Pan, Y J Chang, Y Q Qin, Y Wang, C H Yan, Y Q Sun, X J Huang, X S Zhao
Objective: This study aimed to observe the dynamic changes of NUP98::NSD1 expression before and after allogeneic hematopoietic stem cell transplantation (allo-HSCT) . Moreover, the clinical value of measurable residual disease (MRD) was analyzed. Methods: Sixteen AML patients who were diagnosed with the NUP98::NSD1 fusion gene and received allo-HSCT at Peking University People's Hospital were included. The NUP98::NSD1 fusion gene and leukemia-associated immunophenotype (LAIP) were monitored before and after transplantation to evaluate their MRD status...
December 14, 2023: Zhonghua Xue Ye Xue za Zhi, Zhonghua Xueyexue Zazhi
https://read.qxmd.com/read/38503417/adjuvant-wilms-tumour-1-specific-dendritic-cell-immunotherapy-complementing-conventional-therapy-for-paediatric-patients-with-high-grade-glioma-and-diffuse-intrinsic-pontine-glioma-protocol-of-a-monocentric-phase-i-ii-clinical-trial-in-belgium
#22
JOURNAL ARTICLE
Toon Van Genechten, Maxime De Laere, Jolien Van den Bossche, Barbara Stein, Kim De Rycke, Caroline Deschepper, Katja Hazes, Renke Peeters, Marie-Madeleine Couttenye, Katrien Van De Walle, Ella Roelant, Sabine Maes, Stephanie Vanden Bossche, Sven Dekeyzer, Manon Huizing, Kim Caluwaert, Griet Nijs, Nathalie Cools, Joris Verlooy, Koen Norga, Stijn Verhulst, Sebastien Anguille, Zwi Berneman, Eva Lion
INTRODUCTION: Diffuse intrinsic pontine glioma (DIPG) and paediatric high-grade glioma (pHGG) are aggressive glial tumours, for which conventional treatment modalities fall short. Dendritic cell (DC)-based immunotherapy is being investigated as a promising and safe adjuvant therapy. The Wilms' tumour protein (WT1) is a potent target for this type of antigen-specific immunotherapy and is overexpressed in DIPG and pHGG. Based on this, we designed a non-randomised phase I/II trial, assessing the feasibility and safety of WT1 mRNA-loaded DC (WT1/DC) immunotherapy in combination with conventional treatment in pHGG and DIPG...
March 18, 2024: BMJ Open
https://read.qxmd.com/read/38501593/a-novel-epc1-kdm2b-fusion-in-high-grade-endometrial-stromal-sarcoma
#23
JOURNAL ARTICLE
Katherine M Vroobel, Sana Khalid, Silvia Cavalchini, Ayoma D Attygalle
The spectrum of endometrial stromal sarcoma (ESS) has expanded substantially since the publication of the most recent World Health Organisation (WHO) Classification of Female Genital Tumours and the advent of widely available genomic testing. We describe a uterine mesenchymal tumor harboring a novel EPC1::KDM2B fusion, best classified within the umbrella of high-grade endometrial stromal sarcoma (HGESS). This tumor was composed of a uniform population of spindled cells with some myxoid stroma, a mitotic rate of up to 21/10 high-power fields, and a largely pushing margin with focal vascular invasion...
March 11, 2024: International Journal of Gynecological Pathology
https://read.qxmd.com/read/38499392/predicting-the-prognosis-of-glioma-patients-with-tert-promoter-mutations-and-guiding-the-specific-immune-profile-of-immune-checkpoint-blockade-therapy
#24
JOURNAL ARTICLE
Wenpeng Cao, Jinzhi Lan, Chujiao Hu, Jinping Kong, Limin Xiang, Zhixue Zhang, Yating Sun, Zhirui Zeng, Shan Lei
The telomerase reverse transcriptase promoter (TERTp) is frequently mutated in gliomas. This study sought to identify immune biomarkers of gliomas with TERTp mutations. Data from TCGA were used to identify and validate survival-associated gene signatures, and immune and stromal scores were calculated using the ESTIMATE algorithm. High stromal or immune scores in patients with TERTp-mutant gliomas correlated with shorter overall survival compared to cases with low stromal or immune scores. Among TERTp-mutant gliomas with both high immune and high stromal scores, 213 commonly shared DEGs were identified...
March 18, 2024: Aging
https://read.qxmd.com/read/38498524/responses-of-yield-and-photosynthetic-characteristics-of-rice-to-climate-resources-under-different-crop-rotation-patterns-and-planting-methods
#25
JOURNAL ARTICLE
Hong Yang, Guangyi Chen, Ziyu Li, Wei Li, Yao Zhang, Congmei Li, Mingming Hu, Xingmei He, Qiuqiu Zhang, Conghua Zhu, Fahong Qing, Xianyu Wei, Tian Li, Xuyi Li, Yuyuan Ouyang
Climate is the most important environmental factor influencing yield during rice growth and development. To investigate the relationships between climate and yield under different crop rotation patterns and planting methods, three typical rotation patterns (vegetable-rice (V), rape-rice (R), and wheat-rice (W)) and two mechanical planting methods (mechanical transplanting (T1) and mechanical direct seeding (T2)) were established. The results showed that compared to the V rotation pattern, the average daily temperature (ADT) during the sowing to heading stage increased under both R and W rotation patterns, which significantly shortened the growth period...
February 15, 2024: Plants (Basel, Switzerland)
https://read.qxmd.com/read/38483358/dendritic-cell-vaccination-strategy-for-the-treatment-of-acute-myeloid-leukemia-a-systematic-review
#26
REVIEW
Jamal Motallebzadeh Khanmiri, Mohsen Alizadeh, Sina Esmaeili, Zeinab Gholami, Ali Safarzadeh, Mohammad Khani-Eshratabadi, Amir Baghbanzadeh, Nazila Alizadeh, Behzad Baradaran
BACKGROUND AIMS: Acute myeloid leukemia (AML) is classified as a hematologic malignancy characterized by the proliferation of immature blood cells within the bone marrow (BM), resulting in an aberrant and unregulated cellular growth. The primary therapeutic modalities for AML include chemotherapy and hematopoietic stem cell transplantation. However, it is important to note that these treatments are accompanied by important adverse effects and mortality rates. Therefore, the need for more effective treatment options seems necessary, and dendritic cell (DC) vaccine therapy can be one of these options...
February 24, 2024: Cytotherapy
https://read.qxmd.com/read/38476972/high-expression-of-wt1-and-low-expression-of-p53-in-archived-blocks-of-children-with-wilms-tumor-in-south-western-uganda
#27
JOURNAL ARTICLE
Brian Ssenkumba, Barnabas Atwiine, Yekosani Mitala, Janet Adongo, Samuel Olowo, Rita Nabulya, Amnia Diaz Anaya, Raymond Atwine
PURPOSE: The determination of the presence or absence of anaplasia in Wilms tumor is difficult sometimes creating diagnostic errors and is worsened by the use of neoadjuvant chemotherapy, which causes cellular alterations that may mimic anaplasia. This study described the histological features of Wilms tumor and their association with WT1 and p53 expression in archived specimens in South Western Uganda. PATIENTS AND METHODS: A series of 308 formalin-fixed paraffin-embedded tissue blocks belonging to 85 children were retrospectively recruited in the only public Histopathology laboratory in South Western Uganda...
2024: Cancer Management and Research
https://read.qxmd.com/read/38467982/development-of-immune-cell-therapy-using-t-cells-generated-from-pluripotent-stem-cells
#28
JOURNAL ARTICLE
Hiroshi Kawamoto, Kyoko Masuda, Seiji Nagano
In the field of cancer immunotherapy, the effectiveness of a method in which patient-derived T cells are genetically modified ex vivo and administered to patients has been demonstrated. However, problems remain with this method, such as (1) time-consuming, (2) costly, and (3) difficult to guarantee the quality. To overcome these barriers, strategies to regenerate T cells using iPSC technology are being pursued by several groups in the last decade. The authors have been developing a method by which specific TCR genes are introduced into iPSCs and T cells are generated from those iPSCs (TCR-iPSC method)...
2024: Advances in Experimental Medicine and Biology
https://read.qxmd.com/read/38467769/mutation-order-in-acute-myeloid-leukemia-identifies-uncommon-patterns-of-evolution-and-illuminates-phenotypic-heterogeneity
#29
JOURNAL ARTICLE
Matthew Schwede, Katharina Jahn, Jack Kuipers, Linde A Miles, Robert L Bowman, Troy Robinson, Ken Furudate, Hidetaka Uryu, Tomoyuki Tanaka, Yuya Sasaki, Asiri Ediriwickrema, Brooks Benard, Andrew J Gentles, Ross Levine, Niko Beerenwinkel, Koichi Takahashi, Ravindra Majeti
Acute myeloid leukemia (AML) has a poor prognosis and a heterogeneous mutation landscape. Although common mutations are well-studied, little research has characterized how the sequence of mutations relates to clinical features. Using published, single-cell DNA sequencing data from three institutions, we compared clonal evolution patterns in AML to patient characteristics, disease phenotype, and outcomes. Mutation trees, which represent the order of select mutations, were created for 207 patients from targeted panel sequencing data using 1 639 162 cells, 823 mutations, and 275 samples...
March 11, 2024: Leukemia
https://read.qxmd.com/read/38464925/management-of-retroperitoneal-high-grade-serous-carcinoma-of-unknown-origin-a-case-report
#30
Wen-Lin Hsieh, Dah-Ching Ding
BACKGROUND: Retroperitoneal high-grade serous carcinoma (HGSC) of unknown origin is a sporadic tumor that can originate from ovarian cancer. Herein, we report the case of a woman with retroperitoneal HGSC of unknown origin and describe how she was diagnosed and treated. CASE SUMMARY: A 71-year-old female presented with the tumor marker CA125 elevated to 1041.9 U/mL upon a regular health examination. Computed tomography revealed retroperitoneal lymph node enlargement...
February 26, 2024: World Journal of Clinical Cases
https://read.qxmd.com/read/38460812/comparative-analysis-of-effects-of-conditioned-mediums-obtained-from-2d-or-3d-cultured-mesenchymal-stem-cells-on-kidney-functions-of-diabetic-rats-early-intervention-could-potentiate-transdifferentiation-of-parietal-epithelial-cell-into-podocyte-precursors
#31
JOURNAL ARTICLE
Serbay Ozkan, Basak Isildar, Hakan Sahin, Halil Ibrahim Saygi, Dildar Konukoglu, Meral Koyuturk
AIM: The secretome of mesenchymal stem cells (MSCs) could be a potential therapeutic intervention for diabetes and associated complications like nephropathy. This study aims to evaluate the effects of conditioned mediums (CMs) collected from umbilical cord-derived MSCs incubated under 2-dimensional (2D) or 3D culture conditions on kidney functions of rats with type-I diabetes (T1D). MAIN METHODS: Sprague-Dawley rats were treated with 20 mg/kg streptozocin for 5 consecutive days to induce T1D, and 12 doses of CMs were applied intraperitoneally for 4 weeks...
March 7, 2024: Life Sciences
https://read.qxmd.com/read/38459434/integrated-analysis-of-transcriptome-and-genome-variations-in-pediatric-t-cell-acute-lymphoblastic-leukemia-data-from-north-indian-tertiary-care-center
#32
JOURNAL ARTICLE
Minu Singh, Pankaj Sharma, Prateek Bhatia, Amita Trehan, Rozy Thakur, Sreejesh Sreedharanunni
INTRODUCTION: T-cell acute lymphoblastic leukemia (T-ALL) is a genetically heterogeneous disease with poor prognosis and inferior outcome. Although multiple studies have been perform on genomics of T-ALL, data from Indian sub-continent is scarce. METHODS: In the current study we aimed to identify the genetic variability of T-ALL in an Indian cohort of pediatric (age ≤ 12 years) T-ALL patients (n = 25) by whole transcriptome sequencing along with whole exome sequencing and correlated the findings with clinical characteristics and disease outcome...
March 8, 2024: BMC Cancer
https://read.qxmd.com/read/38450181/case-report-bcr-abl-positive-acute-lymphoblastic-leukemia-with-bone-destruction-a-treatment-dilemma
#33
Shi Lijun, Ma Zhongrui, Wei Li, Yu Xia, Jiang Wei, Pan Yaning
Although bone destruction and hypercalcemia without acute peripheral blast BCR-ABL-positive acute lymphoblastic leukemia (ALL) have been reported in children, they are rare in adults. Herein, we describe a case of BCR-ABL positive ALL with a triploid karyotype, WT1, and CDKN2A mutations with hypercalcemia and bone destruction as the first manifestations. Complete remission (CR) was achieved by induction chemotherapy. BCR-ABL turned negative after treatment with dasatinib. However, computed tomography and whole-body bone scan showed extensive bone destruction...
2024: Frontiers in Oncology
https://read.qxmd.com/read/38440227/case-report-an-unusual-presentation-of-intra-abdominal-desmoplastic-small-round-cell-tumor
#34
Akshay Nilesh Desai, Christine Jane Kurian, William Rafferty, Danielle Lajoie Behrens, Polina Khrizman
BACKGROUND: Intra-abdominal desmoplastic small round cell tumor (IDSRCT) is a rare entity (0.2-0.74 cases per million people per year), which predominantly occurs in young men. It may present as an abdominal mass with pain, distention, and constipation. IDSRCT has a very poor prognosis, with 5-year overall survival estimated at 15%-30%. Diagnosis is made with tissue biopsy. CASE DESCRIPTION: We present a case of a 28-year-old man with a history of schizophrenia and depression who presented to an emergency room (ER) in November 2022 with constipation and pelvic pain...
2024: Frontiers in Oncology
https://read.qxmd.com/read/38437817/is-primary-poorly-differentiated-sarcomatoid-malignancy-of-the-parotid-gland-sarcomatoid-undifferentiated-dedifferentiated-melanoma-report-of-three-unusual-cases-diagnosed-by-fine-needle-aspiration-combined-with-histological-immunohistochemical-and-molecular
#35
JOURNAL ARTICLE
Jerzy Klijanienko, Julien Masliah-Planchon, Olivier Choussy, Guillaume Rougier, Antoine Dubray Vautrin, Maria Lesnik, Nathalie Badois, Wahib Ghanem, Jan Klos, Christophe Le Tourneau, Gregoire Marret, Raymond Barnhill, Adel K El-Naggar
INTRODUCTION: Poorly differentiated primary sarcomatoid parotid malignancies are extremely rare. These tumors have not been consistently studied by morphology, immunohistochemistry or molecular techniques. CASE PRESENTATION: We report three unusual cases of parotid gland poorly-differentiated sarcomatoid malignancy investigated by fine needle aspiration and studied histologically, by immunohistochemistry and molecular investigations. Aspirates showed poorly specific polymorphous sarcomatoid malignancy in all cases...
March 4, 2024: Acta Cytologica
https://read.qxmd.com/read/38427208/decade-long-wt1-specific-ctls-induced-by-wt1-peptide-vaccination
#36
JOURNAL ARTICLE
Tatsuya Suwabe, Yasuhiko Shibasaki, Suguru Tamura, Takayuki Katagiri, Kyoko Fuse, Tori Ida-Kurasaki, Takashi Ushiki, Hirohito Sone, Miwako Narita, Masayoshi Masuko
INTRODUCTION: The peptide-based cancer vaccine targeting Wilms' tumor 1 (WT1) is a promising immunotherapeutic strategy for hematological malignancies. It remains unclear how long and to what extent the WT1-specific CD8 + cytotoxic T cell (CTL) persist after WT1 peptide vaccination. METHODS: The WT1 peptide vaccine was administered with written consent to a patient with CML in the chronic phase who did not respond well to imatinib, and the patient was followed for 12 years after vaccination...
March 1, 2024: International Journal of Hematology
https://read.qxmd.com/read/38426285/-ubtf-tandem-duplications-in-pediatric-myelodysplastic-syndrome-and-acute-myeloid-leukemia-implications-for-clinical-screening-and-diagnosis
#37
JOURNAL ARTICLE
Juan M Barajas, Masayuki Umeda, Lisett Contreras, Mahsa Khanlari, Tamara Westover, Michael P Walsh, Emily Xiong, Chenchen Yang, Brittney Otero, Marc Arribas-Layton, Sherif Abdelhamed, Guangchun Song, Xiaotu Ma, Melvin E Thomas Rd, Jing Ma, Jeffery M Klco
Recent genomic studies in adult and pediatric acute myeloid leukemia (AML) demonstrated recurrent in-frame tandem duplications (TD) in exon 13 of upstream binding transcription factor (UBTF). These alterations, which account for ~4.3% of AMLs in childhood and about 3% in adult AMLs under 60, are subtype-defining and associated with poor outcomes. Here, we provide a comprehensive investigation into the clinicopathological features of UBTF-TD myeloid neoplasms in childhood, including 89 unique pediatric AML and 6 myelodysplastic syndrome (MDS) cases harboring a tandem duplication in exon 13 of UBTF...
February 29, 2024: Haematologica
https://read.qxmd.com/read/38423183/inhibition-of-transcriptional-coactivator-yap-impairs-the-expression-and-function-of-transcription-factor-wt1-in-diabetic-podocyte-injury
#38
JOURNAL ARTICLE
Jianchun Chen, Xiaoyong Wang, Qian He, Hai-Chun Yang, Agnes B Fogo, Raymond C Harris
Podocyte injury and loss are hallmarks of diabetic nephropathy (DN). However, the molecular mechanisms underlying these phenomena remain poorly understood. YAP (Yes-associated protein) is an important transcriptional coactivator that binds with various other transcription factors, including the TEAD family members (nuclear effectors of the Hippo pathway), that regulate cell proliferation, differentiation, and apoptosis. The present study found an increase in YAP phosphorylation at S127 of YAP and a reduction of nuclear YAP localization in podocytes of diabetic mouse and human kidneys, suggesting dysregulation of YAP may play a role in diabetic podocyte injury...
February 27, 2024: Kidney International
https://read.qxmd.com/read/38421713/nkt-licensed-in-vivo-dendritic-cell-based-immunotherapy-as-cellular-immunodrugs-for-cancer-treatment
#39
JOURNAL ARTICLE
Shin-Ichiro Fujii, Kanako Shimizu
With the advent of new therapies, immunotherapy has gained attention as a critical modality. After the discovery of the natural killer T (NKT) cells ligand, ex vivo cultured dendritic cells (DCs) loaded with NKT ligand (especially α-galactosylceramide (α-GalCer) (DC/Gal) or ex vivo expanded NKT transfer studies were clinically examined in several institutes. To prevent tumoral immune escape, the link between innate and adaptive immunity, in situ selective targeting of DCs has been attempted; however, protocol optimization was required...
2024: Critical Reviews in Oncogenesis
https://read.qxmd.com/read/38418687/ovarian-endometrioid-carcinoma-with-a-sex-cord-like-pattern-a-morphological-immunohistochemical-and-molecular-analysis
#40
JOURNAL ARTICLE
Antonio Travaglino, Damiano Arciuolo, Angela Santoro, Caterina Fulgione, Alessia Piermattei, Manuela Martinelli, Maria Elisabetta Onori, Angelo Minucci, Antonio Raffone, Frediano Inzani, Gian Franco Zannoni
Sex cord-like endometrioid carcinoma (SCLEC) is an uncommon entity which may constitute a diagnostic challenge. This study aimed to perform a clinicopathological, immunohistochemical, and molecular reappraisal of ovarian SCLEC. Consecutive ovarian SCLECs cases from a single institution were reviewed during a 13-year period. Twenty-three immunohistochemical markers were tested; 10 genes were analyzed by next-generation sequencing. Nine cases of ovarian SCLEC were identified. Mean patient age was 65.7 years; three cases showed extraovarian extension...
February 29, 2024: Virchows Archiv: An International Journal of Pathology
keyword
keyword
46777
2
3
Fetch more papers »
Fetching more papers... Fetching...
Remove bar
Read by QxMD icon Read
×

Save your favorite articles in one place with a free QxMD account.

×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"

We want to hear from doctors like you!

Take a second to answer a survey question.