Search

The use of biological samples from museum and/or archive collections is common in stable isotope research, particularly for marine mammals. Yet, the temporal stability of isotopic values across various tissue types and the influence of different preservatives on these values are not fully understood, posing significant challenges for accurate data interpretation. Here we examine the impact of three different tissue preservation methods (DMSO, ethanol, freezing), on seven different tissues (blubber, heart, kidney, lung, liver, muscle, and skin) from both a harbor porpoise (Phocoena phocoena) and a gray seal (Halichoerus grypus) for stable isotope analysis in a 1‐year period. Our results demonstrate that storage in DMSO generates greater temporal variability in δ13C and δ15N for all tissue types, particularly in the first six months of storage. Furthermore, tissues stored in DMSO often exhibited lower δ13C and δ15N values compared to those stored frozen or in ethanol. This finding highlights a significant issue for studies utilizing tissues stored in DMSO, regardless of the storage duration. These results underscore the critical need for careful consideration of preservation methods in studies involving stored tissues, providing valuable insights for experimental design and management of tissue archives. [ABSTRACT FROM AUTHOR]

The tumor microenvironment is a determinant of cancer progression and therapeutic efficacy, with nutrient availability playing an important role. Although it is established that the local abundance of specific nutrients defines the metabolic parameters for tumor growth, the factors guiding nutrient availability in tumor compared to normal tissue and blood remain poorly understood. To define these factors in renal cell carcinoma (RCC), we performed quantitative metabolomic and comprehensive lipidomic analyses of tumor interstitial fluid (TIF), adjacent normal kidney interstitial fluid (KIF), and plasma samples collected from patients. TIF nutrient composition closely resembles KIF, suggesting that tissue-specific factors unrelated to the presence of cancer exert a stronger influence on nutrient levels than tumor-driven alterations. Notably, select metabolite changes consistent with known features of RCC metabolism are found in RCC TIF, while glucose levels in TIF are not depleted to levels that are lower than those found in KIF. These findings inform tissue nutrient dynamics in RCC, highlighting a dominant role of non-cancer driven tissue factors in shaping nutrient availability in these tumors., Competing Interests: DECLARATION OF INTERESTS C.S.N. declares royalty income from Cambridge Epigenetix and ThermoFisher (formerly Life Techologies) and stock ownership in Opko Health. R.K.J. received consultant/SAB fees from Cur, DynamiCure, Elpis, SPARC, SynDevRx; owns equity in Accurius, Enlight, SynDevRx; served on the Board of Trustees of Tekla Healthcare Investors, Tekla Life Sciences Investors, Tekla Healthcare Opportunities Fund, Tekla World Healthcare Fund, and received Research Grants from Boehringer Ingelheim and Sanofi; no funding or reagents from these organizations were used in the study. M.G.V.H. discloses that he is a scientific advisor for Agios Pharmaceuticals, iTeos Therapeutics, Sage Therapeutics, Pretzel Therapeutics, Lime Therapeutics, Faeth Therapeutics, Droia Ventures, and Auron Therapeutics. All remaining authors declare no competing interests.