Format

Send to

Choose Destination
Proc Natl Acad Sci U S A. 2017 Oct 24;114(43):11404-11409. doi: 10.1073/pnas.1706617114. Epub 2017 Oct 9.

Human SHMT inhibitors reveal defective glycine import as a targetable metabolic vulnerability of diffuse large B-cell lymphoma.

Author information

1
Department of Chemistry, Princeton University, Princeton NJ 08544.
2
Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton NJ 08544.
3
Department of Molecular Biology, Princeton University, Princeton NJ 08544.
4
Raze Therapeutics, Cambridge, MA 02139.
5
Princeton University Small Molecule Screening Center, Princeton University, Princeton, NJ 08544.
6
Department of Chemistry, Princeton University, Princeton NJ 08544; joshr@princeton.edu.

Abstract

The enzyme serine hydroxymethyltransferse (SHMT) converts serine into glycine and a tetrahydrofolate-bound one-carbon unit. Folate one-carbon units support purine and thymidine synthesis, and thus cell growth. Mammals have both cytosolic SHMT1 and mitochondrial SHMT2, with the mitochondrial isozyme strongly up-regulated in cancer. Here we show genetically that dual SHMT1/2 knockout blocks HCT-116 colon cancer tumor xenograft formation. Building from a pyrazolopyran scaffold that inhibits plant SHMT, we identify small-molecule dual inhibitors of human SHMT1/2 (biochemical IC50 ∼ 10 nM). Metabolomics and isotope tracer studies demonstrate effective cellular target engagement. A cancer cell-line screen revealed that B-cell lines are particularly sensitive to SHMT inhibition. The one-carbon donor formate generally rescues cells from SHMT inhibition, but paradoxically increases the inhibitor's cytotoxicity in diffuse large B-cell lymphoma (DLBCL). We show that this effect is rooted in defective glycine uptake in DLBCL cell lines, rendering them uniquely dependent upon SHMT enzymatic activity to meet glycine demand. Thus, defective glycine import is a targetable metabolic deficiency of DLBCL.

KEYWORDS:

DLBCL; SHMT; cancer metabolism; folate; glycine

PMID:
29073064
PMCID:
PMC5664509
DOI:
10.1073/pnas.1706617114
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center