Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText.
Kick-your-searchterm to multiple Engines kick-your-query now !>
A dictionary by aggregated review articles of nephrology, medicine and the life sciences
Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

suck abstract from ncbi


10.3390/ijms21093351

http://scihub22266oqcxt.onion/10.3390/ijms21093351
suck pdf from google scholar
32397400!7247589!32397400
unlimited free pdf from europmc32397400    free
PDF from PMC    free
html from PMC    free

suck abstract from ncbi


Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534
pmid32397400      Int+J+Mol+Sci 2020 ; 21 (9): ä
Nephropedia Template TP

gab.com Text

Twit Text FOAVip

Twit Text #

English Wikipedia


  • Endoplasmic Reticulum Calcium Pumps and Tumor Cell Differentiation #MMPMID32397400
  • Papp B; Launay S; Gelebart P; Arbabian A; Enyedi A; Brouland JP; Carosella ED; Adle-Biassette H
  • Int J Mol Sci 2020[May]; 21 (9): ä PMID32397400show ga
  • Endoplasmic reticulum (ER) calcium homeostasis plays an essential role in cellular calcium signaling, intra-ER protein chaperoning and maturation, as well as in the interaction of the ER with other organelles. Calcium is accumulated in the ER by sarco/endoplasmic reticulum calcium ATPases (SERCA enzymes) that generate by active, ATP-dependent transport, a several thousand-fold calcium ion concentration gradient between the cytosol (low nanomolar) and the ER lumen (high micromolar). SERCA enzymes are coded by three genes that by alternative splicing give rise to several isoforms, which can display isoform-specific calcium transport characteristics. SERCA expression levels and isoenzyme composition vary according to cell type, and this constitutes a mechanism whereby ER calcium homeostasis is adapted to the signaling and metabolic needs of the cell, depending on its phenotype, its state of activation and differentiation. As reviewed here, in several normal epithelial cell types including bronchial, mammary, gastric, colonic and choroid plexus epithelium, as well as in mature cells of hematopoietic origin such as pumps are simultaneously expressed, whereas in corresponding tumors and leukemias SERCA3 expression is selectively down-regulated. SERCA3 expression is restored during the pharmacologically induced differentiation of various cancer and leukemia cell types. SERCA3 is a useful marker for the study of cell differentiation, and the loss of SERCA3 expression constitutes a previously unrecognized example of the remodeling of calcium homeostasis in tumors.
  • |Biomarkers, Tumor/analysis[MESH]
  • |Breast Neoplasms/enzymology[MESH]
  • |Calcium Signaling[MESH]
  • |Calcium/*metabolism[MESH]
  • |Carcinoma/enzymology[MESH]
  • |Cell Differentiation[MESH]
  • |Cell Line, Tumor[MESH]
  • |Choroid Plexus Neoplasms/enzymology[MESH]
  • |Endoplasmic Reticulum/*metabolism[MESH]
  • |Gastrointestinal Neoplasms/enzymology[MESH]
  • |Gene Expression Regulation, Enzymologic[MESH]
  • |Gene Expression Regulation, Neoplastic[MESH]
  • |Homeostasis[MESH]
  • |Humans[MESH]
  • |Isoenzymes/genetics/metabolism[MESH]
  • |Leukemia, Promyelocytic, Acute/metabolism[MESH]
  • |Lung Neoplasms/enzymology[MESH]
  • |Megakaryocytes/cytology/metabolism[MESH]
  • |Neoplasm Proteins/*metabolism[MESH]
  • |Neoplasms/*metabolism[MESH]
  • |Organ Specificity[MESH]
  • |Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/metabolism[MESH]


  • DeepDyve
  • Pubget Overpricing
  • suck abstract from ncbi

    Linkout box