JCI early table of contents for Dec. 9, 2013

Breast cancer prognosis associated with oncometabolite accumulation

The metabolic profile of cancer cells can be used to develop therapies and identify biomarkers associated with cancer outcome. In this issue of the Journal of Clinical Investigation Stefan Ambs and colleagues at the National Cancer Institute discovered an association between the oncometabolite 2-hydroxyglutarate (2-HG) levels, DNA methylation patterns, and breast cancer prognosis. The authors identified a breast cancer subtype with high levels of 2-HG, and a district DNA methylation pattern that was associated with reduced survival. This breast cancer subtype was common in African-American breast cancer patients, who as a group have a high prevalence of aggressive breast cancers. This study indicates that evaluation of 2-HG along with DNA methylation may be a useful biomarker for breast cancer diagnosis and prognosis

TITLE: MYC-driven accumulation of 2-hydroxyglutarate is associated with breast cancer prognosis

AUTHOR CONTACT: Stefan Ambs National Cancer Institute, Bethesda, MD, USA Phone: 301-496-4668; E-mail: ambss@mail.nih.gov

View this article at: http://www.jci.org/articles/view/71180?key=e428ff2ab0218ea590e1

Choloroquine reduces formation of bone resorbing cells in murine osteoporosis

Bone homeostasis requires precise balance between deposition of new bone by osteoblasts and resorption of old bone by osteoclasts. Bone diseases, including osteoporosis and rheumatoid arthritis, are the result of increased osteoclast activity and formation, which allows bone resorption to outpace deposition. In this issue of the Journal of Clinical Investigation, Brendan Boyce and colleagues at the University of Rochester evaluated the role of TNF receptor–associated receptor 3 (TRAF3) in promoting osteoclast formation. Mice lacking TRAF3 in osteoclast precursor cells had mild osteoporosis that was associated with increased osteoclast formation. The authors found that chloroquine treatment increased TRAF3 in osteoclast precursor cells and limited osteoclast generation. Furthermore, treatment of mouse models of osteoporosis with chloroquine inhibited osteoclast formation. These studies implicate that therapies aimed at increasing TRAF3 in osteoclast precursor cells may limit bone loss for those with bone diseases.

TITLE:Chloroquine reduces osteoclastogenesis in murine osteoporosis by preventing TRAF3 degradation

AUTHOR CONTACT: Brendan Boyce University of Rochester Medical Center, Rochester, NY, USA Phone: 585-275-5837; Fax: 585-276-2832; E-mail: brendan_boyce@urmc.rochester.edu

View this article at: http://www.jci.org/articles/view/66947?key=5187dc887c5491664800

ALSO IN THIS ISSUE

TITLE:

Increased sugar uptake promotes oncogenesis via EPAC/RAP1 and O-GlcNAc pathways

AUTHOR CONTACT:

Mina Bissell

Lawrence Berkeley National Laboratory, Berkeley, CA, USA

Phone: 510 486-4365; E-mail: mjbissell@lbl.gov

View this article at: http://www.jci.org/articles/view/63146?key=7749b0e936bffa996011

TITLE: Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation

AUTHOR CONTACT: Ivan Maillard University of Michigan, Ann Arbor, MI, USA Phone: 734-763-3599; Fax: 734-615-5493; E-mail: imaillar@umich.edu

View this article at: http://www.jci.org/articles/view/67871?key=ca7546ee3f58d0b2e096

TITLE: Embryonic exposure to excess thyroid hormone causes thyrotrope cell death

AUTHOR CONTACT: Ksenia Tonyushkina Baystate Medical Center, Springfield, MA, USA Phone: 413-794-3510; E-mail: ksenia.tonyushkina@bhs.org

View this article at: http://www.jci.org/articles/view/70038?key=4e70d4504e09ce632a0f<\/p>

TITLE:Diverting T helper cell trafficking through increased plasticity attenuates autoimmune encephalomyelitis

AUTHOR CONTACT: Dorina Avram Albany Medical College, Albany, NY, USA Phone: 518-262-6731; E-mail: avramd@mail.amc.edu

View this article at: http://www.jci.org/articles/view/70103?key=9a540eeb2b0b19f8798b

TITLE: Combined SFK/MEK inhibition prevents metastatic outgrowth of dormant tumor cells

AUTHOR CONTACT: Jeff Green National Cancer Institute, Potomac, MD, USA Phone: 301-435-5193; Fax: 301-496-8709; E-mail: jegreen@nih.gov

View this article at: http://www.jci.org/articles/view/70259?key=f6260391d44effc936ab

TITLE: LRIG1 inhibits STAT3-dependent inflammation to maintain corneal homeostasis

AUTHOR CONTACT: Takahiro Nakamura Kyoto Prefectural University of Medicine, Kyoto, , JPN Phone: +81-75-251-5578; Fax: +81-75-251-5663; E-mail: tnakamur@koto.kpu-m.ac.jp

View this article at: http://www.jci.org/articles/view/71488?key=d1957df2c922a9a9a9fb

Source: Journal of Clinical Investigation