Possible fungus-eating cucujiformian beetle larvae with setiferous processes from Cretaceous and Miocene ambers

Beetle larvae represent important components of the modern-day fauna. This should have been the case in the past as well. Yet, fossil beetle larvae are rare, or at least are rare in the literature, as identifying a beetle larva to a narrower taxonomic group is very challenging. This is even more complicated if prominent features have evolved convergently in several lineages. Yet, even in such cases, an ecological interpretation of the fossils is possible if the convergent character is coupled to a specific life habit. For example, different, not closely related, beetle larvae that possess setiferous processes. We here report on three beetle larvae, one from Miocene Mexican and two from Cretaceous Kachin amber, Myanmar. These larvae possess setiferous processes, most similar to the processes of modern representatives of Cucujiformia, especially of the groups Endomychidae, Erotylidae, Cerylonidae and Coccinellidae. Considering the shape of the entire habitus, we see the most similarities between the new larvae and the modern larvae of Endomychidae. However, the new larvae and the larvae of modern representatives differ in certain aspects, most prominently in the body size. The fossils are smaller than their extant counterparts with setiferous processes. Hence the fossils could represent larvae of Endomychidae, but the case remains unclear. Despite this uncertainty, we suggest a lifestyle of the fossil larvae as fungus-eaters on rotting wood. This lifestyle is not only known from extant larvae of Endomychidae, but also from other larvae with similar processes

Age-Related Co-Expression of BCOR and BCORL1 mRNA in Acute Myeloid Leukemia

Background: Acute myeloid leukemia (AML) is an aggressive hematological malignancy caused by a variety of genetic abnormalities and epigenetic dysregulation. The incidence of AML is strongly related to age, with the highest incidence rates being in older adults. The loss of function mutations in BCOR and BCORL1 genes have been identified in AML. BCL6 corepressor (BCOR) and BCL6 corepressor like 1 (BCORL1) are important epigenetic regulators as a member of Polycomb repressive complex 1 (PRC1.1), involved in histone modification processes

Elevación de SPINK2 en leucemia mieloide aguda

La leucemia mieloide aguda (AML, por sus siglas en inglés) es una enfermedad muy heterogénea. Aunque se puede clasificar a los pacientes en grupos de riesgo según sus mutaciones genéticas, el pronóstico dentro de cada categoría varía sustancialmente. Es perentorio identificar nuevos marcadores moleculares de la AML. Recientemente, se ha descrito la elevación del inhibidor de la serina peptidasa Kazal tipo 2 (SPINK2) en la AML, habiendo sido relacionada con peores resultados clínicos en metaanálisis, así como en un número limitado de pacientes con AML

Upregulation of SPINK2 in acute myeloid leukemia

Acute myeloid leukemia (AML) is a highly heterogeneous disease. Although patients can be classified into risk groups based on their genetic changes, the prognosis of disease within these categories varies widely. This situation raises the need to search for new molecular markers related to AML. Serine peptidase inhibitor Kazal type 2 (SPINK2) has recently been reported to be upregulated in AML and associated with poor outcomes by meta-analysis and in a limited number of AML patients

Elevación de SPINK2 en leucemia mieloide aguda

La leucemia mieloide aguda (AML), una patolog a maligna progresiva, es un trastorno de las c lulas madre hematopoy ticas caracterizada por un incremento en el n mero de c lulas mieloides de la m dula sea y el bloqueo de su maduraci n. Su incidencia aumenta con la edad [1, 2]. La AML es heterog nea en t rminos gen ticos, biol gicos y cl nicos. Algunas de las alteraciones gen ticas observadas en la AML consisten en alteraciones cromos micas, tales como la p rdida de parte o la totalidad de chr 5 y ch 7, t(15;17)(q22;q12), t(8;21)(q22;q22.1), inv(16)(p13.1q22)/ t(16;16)(p13.1;q22), inv(3)(q21.3q26.2)/t(3;3)(q21.3;q26.2), t(6;9)- (p23;q34.1), t(9;11)(p21.3;q23.3) y t(1;22)(p13.3;q13.3) [3]. Aparte de dichas alteraciones cromos micas, las mutaciones m s comunes se producen en los genes FLT3, NPM1, DNMT3A, KIT, CEBPA, RUNX1, IDH1/2 TET2 ve MLL, ASLX1, BCOR, BCORL1, TP53, GATA2, DDX41, KMT2A, SRP72 y STAG2 [4, 5

Castleman Disease: A Multicenter Case Series from Turkey

Objective: Castleman disease (CD) is a rare disease also known as angiofollicular lymph node hyperplasia. The two main histological subtypes are the hyaline vascular and plasma cell variants. It is further classified as unicentric CD (UCD) or multicentric CD (MCD) according to the anatomical distribution of the disease and the number of lymph nodes involved. The aim of this multicenter study was to evaluate all cases of CD identified to date in Turkey to set up a national registry to improve the early recognition, treatment, and follow-up of CD. Materials and Methods: Both adult (n=130) and pediatric (n=10) patients with lymph node or involved field biopsy results reported as CD were included in the study. Patients’ demographic information, clinical and laboratory characteristics, imaging study results, treatment strategies, and clinical outcomes were evaluated retrospectively. Results: A total of 140 patients (69 male and 71 female) with a diagnosis of UCD (n=73) or MCD (n=67) were included. The mean age was 39 years in the UCD group and 47 years in the MCD group. Female patients were more common in the UCD group. The most common histological subtype was hyaline vascular for both UCD and MCD patients. Asymptomatic patients were more common in the UCD group. Anemia, elevations of acute phase reactants, and hypoalbuminemia were more common in the MCD group. The most commonly used treatment strategies for UCD were surgical excision, rituximab, and radiotherapy, respectively. All UCD patients were alive at a median of 19.5 months of follow-up. The most commonly used treatment strategies for MCD were methyl prednisolone, R-CHOP, R-CVP, and rituximab. Thirteen MCD patients had died at a median of 34 months of follow-up. Conclusion: This study is important in presenting the patient characteristics and treatment strategies for CD from Turkey, with the potential of increasing awareness about CD. Treatment data may help in making decisions, particularly in countries that do not have access to siltuximab. However, larger prospective studies are needed to make definitive conclusions. © 2022 by Turkish Society of Hematology.Türk Hematoloji Derneğisupported by the Turkish Society of Hematology

Castleman Disease: A Multicenter Case Series from Turkey.

Objective: Castleman disease (CD) is a rare disease also known as angiofollicular lymph node hyperplasia. The two main histological subtypes are the hyaline vascular and plasma cell variants. It is further classified as unicentric CD (UCD) or multicentric CD (MCD) according to the anatomical distribution of the disease and the number of lymph nodes involved. The aim of this multicenter study was to evaluate all cases of CD identified to date in Turkey to set up a national registry to improve the early recognition, treatment, and follow-up of CD. Materials and Methods: Both adult (n=130) and pediatric (n=10) patients with lymph node or involved field biopsy results reported as CD were included in the study. Patients' demographic information, clinical and laboratory characteristics, imaging study results, treatment strategies, and clinical outcomes were evaluated retrospectively. Results: A total of 140 patients (69 male and 71 female) with a diagnosis of UCD (n=73) or MCD (n=67) were included. The mean age was 39 years in the UCD group and 47 years in the MCD group. Female patients were more common in the UCD group. The most common histological subtype was hyaline vascular for both UCD and MCD patients. Asymptomatic patients were more common in the UCD group. Anemia, elevations of acute phase reactants, and hypoalbuminemia were more common in the MCD group. The most commonly used treatment strategies for UCD were surgical excision, rituximab, and radiotherapy, respectively. All UCD patients were alive at a median of 19.5 months of follow-up. The most commonly used treatment strategies for MCD were methyl prednisolone, R-CHOP, R-CVP, and rituximab. Thirteen MCD patients had died at a median of 34 months of follow-up. Conclusion: This study is important in presenting the patient characteristics and treatment strategies for CD from Turkey, with the potential of increasing awareness about CD. Treatment data may help in making decisions, particularly in countries that do not have access to siltuximab. However, larger prospective studies are needed to make definitive conclusions