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Characterization of metabolic alterations of chronic lymphocytic leukemia in the lymph node microenvironment

Characterization of metabolic alterations of chronic lymphocytic leukemia in the lymph node microenvironment
Characterization of metabolic alterations of chronic lymphocytic leukemia in the lymph node microenvironment
Altered metabolism is a hallmark of both cell division and cancer. Chronic lymphocytic leukemia (CLL) cells circulate between peripheral blood (PB) and lymph nodes (LNs), where they receive proliferative and prosurvival signals from surrounding cells. However, insight into the metabolism of LN CLL and how this may relate to therapeutic response is lacking. To obtain insight into CLL LN metabolism, we applied a 2-tiered strategy. First, we sampled PB from 8 patients at baseline and after 3-month ibrutinib (IBR) treatment, which forces egress of CLL cells from LNs. Second, we applied in vitro B-cell receptor (BCR) or CD40 stimulation to mimic the LN microenvironment and performed metabolomic and transcriptomic analyses. The combined analyses indicated prominent changes in purine, glucose, and glutamate metabolism occurring in the LNs. CD40 signaling mostly regulated amino acid metabolism, tricarboxylic acid cycle (TCA), and energy production. BCR signaling preferably engaged glucose and glycerol metabolism and several biosynthesis routes. Pathway analyses demonstrated opposite effects of in vitro stimulation vs IBR treatment. In agreement, the metabolic regulator MYC and its target genes were induced after BCR/CD40 stimulation and suppressed by IBR. Next, 13C fluxomics performed on CD40/BCR-stimulated cells confirmed a strong contribution of glutamine as fuel for the TCA cycle, whereas glucose was mainly converted into lactate and ribose-5-phosphate. Finally, inhibition of glutamine import with V9302 attenuated CD40/BCR-induced resistance to venetoclax. Together, these data provide insight into crucial metabolic changes driven by the CLL LN microenvironment. The prominent use of amino acids as fuel for the TCA cycle suggests new therapeutic vulnerabilities.
0006-4971
630-643
Chen, Zhenghao
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Simon-Molas, Helga
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Cretenet, Gaspard
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Valle-Argos, Beatriz
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Smith, Lindsay D.
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Forconi, Francesco
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Schomakers, Bauke V.
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van Weeghel, Michel
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Bryant, Dean J.
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van Bruggen, Jaco A.C.
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Peters, Fleur S.
303a2901-5f0d-4822-aa87-b0c882547e9e
Rathmell, Jeffrey C.
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van der Windt, Gerritje J.W.
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Kater, Aron P.
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Packham, Graham
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Eldering, Eric
3ceb48b0-8d2c-47b6-b8a0-0aff486e2e0f
Chen, Zhenghao
514f6ae4-2696-4917-aea8-12f700a007d5
Simon-Molas, Helga
2db02363-19a5-459e-aec5-a1cf774a8abf
Cretenet, Gaspard
83ec7165-7aac-490a-ae2a-15aa5ab89f4d
Valle-Argos, Beatriz
4fddaa71-c0aa-4b95-b464-8bdb592428a2
Smith, Lindsay D.
1d44c2d0-d5af-411e-b6cd-9b5633f2eb1e
Forconi, Francesco
ce9ed873-58cf-4876-bf3a-9ba1d163edc8
Schomakers, Bauke V.
c26b783b-c3be-4417-b75f-39e953a1e164
van Weeghel, Michel
6b3753ea-02d8-45b4-ae2d-353e8f4991fc
Bryant, Dean J.
10ed83e8-8080-4d9c-bba5-df9d4eec3a10
van Bruggen, Jaco A.C.
a0beb2ef-34c4-43a1-8845-97483904ac45
Peters, Fleur S.
303a2901-5f0d-4822-aa87-b0c882547e9e
Rathmell, Jeffrey C.
8538575b-6a7b-4393-a258-f1675ebb813c
van der Windt, Gerritje J.W.
245a3087-7727-4371-bb44-0ece5fd22cb3
Kater, Aron P.
b0c9bb11-e6e5-4c8f-be47-a0b63aca2073
Packham, Graham
fdabe56f-2c58-469c-aadf-38878f233394
Eldering, Eric
3ceb48b0-8d2c-47b6-b8a0-0aff486e2e0f

Chen, Zhenghao, Simon-Molas, Helga, Cretenet, Gaspard, Valle-Argos, Beatriz, Smith, Lindsay D., Forconi, Francesco, Schomakers, Bauke V., van Weeghel, Michel, Bryant, Dean J., van Bruggen, Jaco A.C., Peters, Fleur S., Rathmell, Jeffrey C., van der Windt, Gerritje J.W., Kater, Aron P., Packham, Graham and Eldering, Eric (2022) Characterization of metabolic alterations of chronic lymphocytic leukemia in the lymph node microenvironment. Blood, 140 (6), 630-643. (doi:10.1182/blood.2021013990).

Record type: Article

Abstract

Altered metabolism is a hallmark of both cell division and cancer. Chronic lymphocytic leukemia (CLL) cells circulate between peripheral blood (PB) and lymph nodes (LNs), where they receive proliferative and prosurvival signals from surrounding cells. However, insight into the metabolism of LN CLL and how this may relate to therapeutic response is lacking. To obtain insight into CLL LN metabolism, we applied a 2-tiered strategy. First, we sampled PB from 8 patients at baseline and after 3-month ibrutinib (IBR) treatment, which forces egress of CLL cells from LNs. Second, we applied in vitro B-cell receptor (BCR) or CD40 stimulation to mimic the LN microenvironment and performed metabolomic and transcriptomic analyses. The combined analyses indicated prominent changes in purine, glucose, and glutamate metabolism occurring in the LNs. CD40 signaling mostly regulated amino acid metabolism, tricarboxylic acid cycle (TCA), and energy production. BCR signaling preferably engaged glucose and glycerol metabolism and several biosynthesis routes. Pathway analyses demonstrated opposite effects of in vitro stimulation vs IBR treatment. In agreement, the metabolic regulator MYC and its target genes were induced after BCR/CD40 stimulation and suppressed by IBR. Next, 13C fluxomics performed on CD40/BCR-stimulated cells confirmed a strong contribution of glutamine as fuel for the TCA cycle, whereas glucose was mainly converted into lactate and ribose-5-phosphate. Finally, inhibition of glutamine import with V9302 attenuated CD40/BCR-induced resistance to venetoclax. Together, these data provide insight into crucial metabolic changes driven by the CLL LN microenvironment. The prominent use of amino acids as fuel for the TCA cycle suggests new therapeutic vulnerabilities.

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More information

Accepted/In Press date: 6 April 2022
e-pub ahead of print date: 29 April 2022

Identifiers

Local EPrints ID: 495763
URI: http://eprints.soton.ac.uk/id/eprint/495763
ISSN: 0006-4971
PURE UUID: 8e387ed3-2602-4703-aa93-b8ece8f29417
ORCID for Francesco Forconi: ORCID iD orcid.org/0000-0002-2211-1831
ORCID for Dean J. Bryant: ORCID iD orcid.org/0000-0003-3163-608X
ORCID for Graham Packham: ORCID iD orcid.org/0000-0002-9232-5691

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Date deposited: 21 Nov 2024 17:53
Last modified: 23 Nov 2024 02:47

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Contributors

Author: Zhenghao Chen
Author: Helga Simon-Molas
Author: Gaspard Cretenet
Author: Beatriz Valle-Argos
Author: Lindsay D. Smith
Author: Bauke V. Schomakers
Author: Michel van Weeghel
Author: Dean J. Bryant ORCID iD
Author: Jaco A.C. van Bruggen
Author: Fleur S. Peters
Author: Jeffrey C. Rathmell
Author: Gerritje J.W. van der Windt
Author: Aron P. Kater
Author: Graham Packham ORCID iD
Author: Eric Eldering

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