Editors' ChoiceCellular and Molecular Signaling

Papers of note in Nature 546 (7659)

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Science Signaling  27 Jun 2017:
Vol. 10, Issue 485, eaao1820
DOI: 10.1126/scisignal.aao1820

This week’s articles describe engineered exosomes for treating pancreatic cancer, the role of the endoplasmic reticulum in cancer cell apoptosis, the priming of brown fat for cold-induced thermogenesis, synapse loss in a mouse model of lupus, and communication between cells of different lineages during liver development.


Targeting pancreatic cancer with exosomes

Kamerkar et al. engineered exosomes carrying an interfering RNA that targets an oncogenic form of KRAS commonly found in pancreatic cancer.

Endoplasmic reticulum calcium flux in cancer

Bononi et al. found that the tumor suppressor BRCA1-associated protein 1 (BAP1) promotes the release of Ca2+ from the endoplasmic reticulum and subsequent apoptosis by stabilizing an IP3 receptor.

Kuchay et al. report that inhibiting ubiquitin-dependent degradation of an IP3 receptor sensitizes PTEN-deficient tumors to photoradiation therapy by restoring the apoptosis-promoting release of Ca2+ from the endoplasmic reticulum.


Priming the thermogenesis machinery

Emmett et al. found that histone deacetylase 3 (HDAC3) primes brown fat to generate heat in response to cold temperature.


How lupus causes synapse loss

Bialas et al. report that interferons promote the loss of synapses in the brain in a mouse model of lupus by stimulating microglia to become reactive (see also McGlasson and Hunt).


Interlineage communication in liver development

Using three-dimensional organoids, Camp et al. demonstrate that vascular endothelial growth factor (VEGF) signaling mediates crosstalk between different cell lineages during liver bud development.

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