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  • American Association for Cancer Research (AACR)  (5)
  • 1
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 78, No. 13_Supplement ( 2018-07-01), p. 774-774
    Abstract: The anti-Müllerian hormone (AMH) belongs to the TGF-β family and plays a key role during fetal sexual development. It has been shown that AMH inhibits proliferation and induces apoptosis of AMH type II receptor (AMHRII) -positive tumor cells, especially progenitor cancer cells. Moreover, various reports have described the expression of AMHRII in human gynecologic cancers including ovarian tumors. Based on qRT-PCR test results, which were confirmed by a specific In-Situ Hybridization (ISH) assay, AMHRII mRNA could be detected only in normal ovary, testis and adrenal gland tissue, and at lower levels in pancreas and stomach. However, when a tissue microarray of solid tumor samples was tested with ISH assay, AMHRII mRNA was surprisingly detected in several primary cancer tissues including melanoma, lung, head and neck, colorectal and breast cancers. For example, a large ISH study involving 58 colorectal cancer samples demonstrated AMHRII expression in 55% of cases. AMHRII protein expression was confirmed by ImmunoHistoChemistry (IHC) in gynecological cancer samples including 179 out of 210 (85%) Granulosa Cell Tumor samples and 55 out of 80 (69 %) Epithelial Ovarian Cancers. In patients with gynecological cancers pre-screened by IHC for inclusion in a Phase Ia/Ib clinical trial of GM102, an anti-AMHRII monoclonal antibody, AMHRII positive membrane expression was detected in 116 out of 166 (70%) archived tumor tissues. Using the same IHC protocol, over 1000 frozen samples covering 16 different cancer types were tested, which demonstrated AMHRII expression in over 50% of hepatocarcinoma, colorectal, lung and renal cancer samples. No AMHRII expression was observed in 75 neuroendocrine lung tumor samples nor in 18 non-Hodgkin lymphoma samples tested. On a small panel of frozen ovarian (11) and colorectal (9) cancer samples using an immunofluorescence assay with an AlexaFluor488-conjugated GM102 antibody, AMHRII expression was confirmed on the matching fresh tissue samples, previously detected by IHC in their fixed counterpart samples. Preliminary FACS analysis of fresh ovarian and colorectal tumor samples have demonstrated comparable expression levels with mean values of 50,000 and 40,000 AMHRII receptors per cell, respectively. In conclusion, the results presented above, using a variety of detection methods and systems, have consistently shown that AMHRII is expressed in many different histological types of solid tumors. These results suggest that this embryonic receptor could be a suitable target for selective antitumor agents such as GM102. Citation Format: Jean-Marc M. Barret, Didier Meseure, Guillaume Bataillon, Noora Andersson, Aurélie Auguste, Olivier Dubreuil, Anniina Färkkilä, Emeline Perrial, Celine Bossard, Emily Loison, Anne Jarry, André Nicolas, Fanny Lemée, Solenne Gaillard, Mehdi Lahmar, Mikko Anttonen, Gabriel Champenois, Charles Dumontet, Isabelle Ray-Coquard, Alexandra Leary, Isabelle Tabah-Fisch, Anne Vincent-Salomon, Jean-François F. Prost. Anti-Müllerian hormone type II receptor (AMHRII) found expressed in human non-gynecological solid tumors, suggesting potential broader applications for anti-AMHRII-based therapy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2018; 2018 Apr 14-18; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2018;78(13 Suppl):Abstract nr 774.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2018
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  • 2
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 64, No. 12 ( 2004-06-15), p. 4227-4234
    Abstract: Mounting evidence suggests that the position in the cell cycle of cells exposed to an oxidative stress could determine their survival or apoptotic cell death. This study aimed at determining whether nitric oxide (NO)-induced cell death in colon cancer cells might depend on their position in the cell cycle, based on a clone of the cancer cell line HT29 exposed to an NO donor, in combination with the manipulation of the cell entry into the cell cycle. We show that PAPA NONOate (pNO), from 10−4 m to 10−3 m, exerted early and reversible cytostatic effects through ribonucleotide reductase inhibition, followed by late resumption of cell growth at 5 × 10−4 m pNO. In contrast, 10−3 m pNO led to late programmed cell death that was accounted for by the progression of cells into the cell cycle as shown by (a) the accumulation of apoptotic cells in the G2-M phase at 10−3 m pNO treatment; and (b) the prevention of cell death by inhibiting the entry of cells into the cell cycle. The entry of pNO-treated cells into the G2-M phase was associated with actin depolymerization and its S-glutathionylation in the same way as in control cells. However, the pNO treatment interfered with the build-up of a high reducing power, associated in control cells with a dramatic increase in reduced glutathione biosynthesis in the G2-M phase. This oxidative stress prevented the exit from the G2-M phase, which requires a high reducing power for actin deglutathionylation and its repolymerization. Finally, our demonstration that programmed cell death occurred through a caspase-independent pathway is in line with the context of a nitrosative/oxidative stress. In conclusion, this work, which deciphers the connection between the position of colonic cancer cells in the cell cycle and their sensitivity to NO-induced stress and their programmed cell death, could help optimize anticancer protocols based on NO-donating compounds.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2004
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  • 3
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 78, No. 13_Supplement ( 2018-07-01), p. 4061-4061
    Abstract: In colorectal cancer (CRC), little is known about mechanisms by which tumor cells can influence the biology of Tumor Infiltrating T lymphocytes (TILs) present in the tumor microenvironment. One of these mechanisms could be modulation of the inflammasome of tumor cells. The inflammasome is a molecular platform present in normal intestinal epithelial cells, whose effector protein, caspase-1, can rapidly mature IL-18 and generate a mucosal Th1 (IFNγ) response. However, the inflammasome status of tumor cells in CRC and its potential role in the biology of TILs are unknown yet. This prospective study aimed to determine in CRC patients (n = 50) : i) the status of the inflammasome (caspase-1 / IL-18 axis) in tumor cells according to their microsatellite status [unstable (MSI) or stable (MSS)], in relation with the density of Th1/Tc1 TILs (T-bet+) and with the levels of the prototype Th1 cytokine IFNγ, secreted in an ex vivo explant culture model of CRC we developed and ii) the impact of the inflammasome-dependent cytokines potentially secreted by tumor cells on the biology of isolated TILs. Our study delineates two major groups of patients. The first group (33% of cases, mostly MSS with a low immunoscore) featured no active caspase-1 in tumor cells, no or low levels of mature IL-18 and IFNγ and only few T-bet+ TILs in the tumor microenvironment. This profile could correspond to an immune escape mechanism facilitating tumor progression. The second group (66% of cases, both MSI and MSS with high immunoscore) featured active caspase-1 in tumor cells associated with mature IL-18 secretion, high density of T-bet+ TILs expressing IL-18Rα and IFNγ release in most cases. In addition, isolated IL-18Rα+ TILs cultured with recombinant IL-18 were able to secrete IFNγ, either left unstimulated or stimulated with anti-CD3. In these CRC, the inflammasome of tumor cells, maintained and active, can contribute to a Th1/Tc1 antitumor response elicited by TILs present in the microenvironment that can modulate tumor growth. Interestingly, in a few cases of this second group (MSI CRC), the numerous T-bet+ TILs were unable to generate a Th1 response. Noticeably, these TILs express numerous immune checkpoints including PD1 and TIGIT, potentially responsible for their exhaustion. This study is the first to delineate functional interactions between tumor cells and TILs in CRC, using ex vivo explant cultures. Altogether, our findings support the inflammasome of tumor cells as a potential new therapeutic target to strengthen the Th1/Tc1 immune response in CRC, in association with immune checkpoint blockers. This work is supported by the “Ligue contre le Cancer Grand Ouest” Citation Format: Linda Bilonda, Delphine Dansette, Cecile Deleine, Romain Oger, Nicolas Jouand, Juliette Podevin, Pierre Fourquier, Emilie Thibaudeau, Jerome Chetritt, Jean-François Mosnier, Celine Bossard, Nadine Gervois, Anne Jarry. The inflammasome of tumor cells modulates the biology of tumor-infiltrating T lymphocytes in colorectal cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2018; 2018 Apr 14-18; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2018;78(13 Suppl):Abstract nr 4061.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2018
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  • 4
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 78, No. 13_Supplement ( 2018-07-01), p. LB-142-LB-142
    Abstract: Background. We have previously demonstrated that overexpression of the human MHC class Ib molecule - HLA-E/β2 microglobulin (β2m) - by tumor cells in colorectal carcinomas (CRC) was associated with an unfavorable prognosis, suggesting its involvement in tumor immune escape. However, the type of specific receptor of HLA-E/β2m expressed by tumor-infiltrating lymphocytes (TILs) - i.e inhibitory CD94/NKG2A or activating CD94/NKG2C - remains unknown yet in CRC. Aims. We retrospectively investigated in the primary tumor of 245 CRC patients 1) the association of HLA-E/β2m overexpression and the density of CD94+ intraepithelial TILs (IEL-TILs) by immunohistochemistry with the microsatellite status of CRC, and 2) the prognostic influence of CD94+ IEL-TILs. We then further analyzed the cell type of CD94+ TIL and the type of receptor expressed - CD94/NKG2A or CD94/NKG2C - by FACS analysis from 19 freshly resected CRC tumors prospectively included. Results. HLA-E/β2m was preferentially overexpressed in microsatellite unstable (MSI) CRC compared with microsatellite stable (MSS) CRC (44,6 % vs 18,4 % respectively, p=0.0001), and was significantly associated with a high density of CD94+ IEL-TIL in MSI (0,9% in HLA-E/β2m+ vs 0,2% in HLA-E/β2m- CRC, p=0,001), but also in MSS CRC (0,38% in HLA-E/β2m+ vs 0,15% in HLA-E/β2m- CRC, p & lt;0,0001). These CD94+ TILs mostly corresponded to αβ (50% among CD94+ cells) and CD8+ (80%) T cells, but 25% corresponded to NK cells. Both CD94+ T and NK cells preferentially expressed the inhibitory NKG2A chain, irrespective of the microsatellite status. Finally, a high density of CD94+ IEL-TILs was independently associated with a worse overall survival (p=0.03). Conclusion. These results strongly suggest that tumor cells/immune cells interactions mediated by HLA-E/β2m and CD94/NKG2A, preferentially upregulated in MSI CRC but also found in a subset of MSS CRC, could represent a promising new druggable inhibitory immune checkpoint targeted by the anti-NKG2A monoclonal antibody (monalizumab). Citation Format: Juliette EUGENE, Nicolas JOUAND, Delphine DANSETTE, Guillaume MEURETTE, Juliette Podevin, Tamara MATYSIAK, Stephane BEZIEAU, Christelle VOLTEAU, Wassila EL ALAMI THOMAS, Jerome CHETRITT, Olivier KERDRAON, Pierre Fourquier, Emilie THIBAUDEAU, Frederic DUMONT, Jean-Francois MOSNIER, Claire TOQUET, Anne JARRY, Nadine GERVOIS, Celine Bossard. CD94/NKG2A+ tumor-infiltrating lymphocytes in a context of HLA-E overexpression could be a promising new druggable inhibitory immune checkpoint in colorectal adenocarcinomas [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2018; 2018 Apr 14-18; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2018;78(13 Suppl):Abstract nr LB-142.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2018
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    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
    Location Call Number Limitation Availability
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  • 5
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 82, No. 12_Supplement ( 2022-06-15), p. 44-44
    Abstract: Large chromosomal alterations are common in cancer and often show preferential gain or loss across many cancer types indicating their selective advantage. Triple negative breast cancer (TNBC) exhibits complex mutational spectrum without common oncogenic drivers yet displays consistent loss of large chromosomal regions. Here, we characterize selection pressures that maintain a recurrently deleted region of chromosome 4p in TNBC. We used single cell and bulk WGS phylogenetic analysis of TNCB PT/PDX panel to show that chr4p deletion is an early event in tumor evolution. We used scRNAseq gene expression and inferred copy number analysis to show that chr4p loss is associated with a proliferative state. This finding was confirmed by a combination of RNA in situ hybridization and immunofluorescence. We then tested the dosage sensitivity of genes residing within this region by individual and dual overexpression in TNBC PDX-derived cell lines and control normal cell line by assessing their effect on cell proliferation. The overexpression of genes within chr4p elicited a strong cell proliferation defect in cancer but not normal cell line models. We also characterized an unknown gene within chr4p region as a novel member of the STRIPAK complex. Genome-wide pooled ORFeome library screens identified a global pattern of background-specific dosage sensitive regions. Our study shows that large chromosomal deletions are maintained due to evolutionary early genetic network rewiring rendering multiple genes within such regions to be dosage sensitive. Ultimately, this work enhances our understanding of genetic events that modulate TNBC. Citation Format: Elena Kuzmin, Jean Monlong, Mathieu Bourgey, Jarry Barber, Tom Lesluyes, Toby Baker, Genevieve Morin, Dongmei Zou, Michael Schwartz, Yang Yang, Alain Pacis, Constanza Martinez, Hellen Kuasne, Anne-Marie Fortier, Rui Li, Claudia Kleinman, Sidong Huang, Peter van Loo, Quaid Morris, Jiannis Ragoussis, Guillaume Bourque, Morag Park. Evolution of large copy number variants in breast cancer through genetic network rewiring [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 44.
    Type of Medium: Online Resource
    ISSN: 1538-7445
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2022
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