Biology subjects

McDaniel, N.

Publications and source records attributed to McDaniel, N..

2 recordsLinked to original sources

bioRxiv2024

Some new Haliclona species (Demospongiae, Haplosclerida) from British Columbia Shallow Waters and a Re-Description of Haliclona mollis (Lambe, 1893)

BackgroundA numer of Haliclona species (Demospongiae, Haplosclerida) in the Austin and McDaniel collections at the Royal British Columbia Museum (RBCM) are identified only to genus or genus and species. The collections are representative of over 40 years of sampling principally by the late Dr. William C. Austin and one of us (Neil McDaniel) through SCUBA diving on the west coast of British Columbia and specimens provided by others to Dr. Austin. We have selected representative Haliclona species in the collections for detailed examination and placement in subgenera and species (where species were not identified). Haliclona is recognized to have several subgenera, thus identification of specimens to genus and species is incomplete. Our study updates this status for the species examined. MethodsMethods of collection included intertidal scrapings or removal of non-encrusting specimens usually accompanied by in-situ photos, similar methods at SCUBA diving depths (subtidal to 35 m) and from other dredging, trawling and biological sampling activities. ResultsWe describe eleven new Haliclona (Demospongeae Haplosclerida Chalinadae) species and a range extension for Haliclona (Flagellia) edaphus de Laubenfels, 1930 for shallow waters of Southwestern British Columbia, Canada. New species include Haliclona (Gellius) hartmani n. sp., Haliclona (Gellius) shishalhensis n. sp., Haliclona (Reniera) gesteta n. sp., Haliclona (Rhizoniera) aborescens n. sp., Haliclona (Rhizoniera) blanca n. sp., Haliclona (Rhizoniera) boothensis n. sp., Haliclona (Rhizoniera) filix n. sp., Haliclona (Rhizoniera) kunechina n.sp., Haliclona (Rhizoniera) meandrina n. sp., Haliclona (Rhizoniera) penelakuta n. sp., and Haliclona (Rhizoniera) vulcana n. sp. We also redescribe Haliclona mollis (Lambe, 1893 [1894]) and propose placing it in the subgenus Haliclona. Except for Lambes syntype slides of Haliclona mollis which are deposited at the Canadian Museum of Nature, Ottawa, Canada, all holotypes and voucher specimens of species described are deposited at RBCM.

zoology↗

bioRxiv2020

The Ephrin receptor A2 and Roundabout Guidance Receptor 1 heterodimer: A potential theranostic for squamous cell carcinomas

Squamous cell carcinomas (SCC) of the lung (LSCC) and head and neck (HNSCC) are very prevalent with poor prognosis and limited treatment options. In both cancer types, Ephrin receptor A2 (EPHA2) is known to be overexpressed and exhibit opposing effects via two distinct signaling mechanisms. While it can inhibit cancer cell survival and migration by ligand-dependent signaling through tyrosine kinase phosphorylation at Y588 and Y772, it can promote tumor progression and cell migration in a ligand-independent manner via phosphorylation at S897. Variable ABnormal morphology (VAB-1) is the C. elegans ortholog of the human ephrin receptor (EPHR) that interacts genetically and biochemically in a dose-dependent manner with the axon guidance receptor, SAX3, the worm ortholog of ROBO. Double mutants of vab-1(EPHR)/sx-3(ROBO) are synthetic lethal, underscoring the interaction between the two signaling pathways which prompted us to investigate their role in SCC. Using biochemical and biophysical techniques, we show that EPHA2 and ROBO1 reside in the same complex and interact physically to form a functional heterodimer in LSCC and HNSCC. Furthermore, we show that treating squamous cells with the SLIT2, ligand of ROBO1, hinders phosphorylation of EPHA2 at S897, and thereby, attenuates cell proliferation. Interestingly, SLIT2 can interact with EPHA2 and attenuate the proliferation of cells that have low ROBO1 expression. Additionally, SLIT2 can act synergistically with the EPHA2 inhibitor, Ensartinib to attenuate cell growth in LSCC and HNSCC cells. Taken together, the data suggest that SLIT2 may serve as a novel therapeutic for LSCC and HNSCC. Here, we propose to stratify patients for treatment with SLIT2 and/or Ensartinib, based on their EPHA2 and ROBO1 expression levels in the diseased tissue. Thus 85% of LSCC cases can be treated with combination of SLIT2+Ensartinib and 55% of HNSCC cases can be treated with either SLIT2 or Ensartinib. Furthermore, EPHA2 and ROBO1 may represent novel theranostics in these two diseases. One sentence summaryHeterodimerization of EPHA2 and ROBO1 receptors attenuates growth of squamous cell carcinomas of the lung and head and neck.

cancer biology↗