- Research article
- Open Access
Functional p53 is required for rapid restoration of daunorubicin-induced lesions of the spleen
BMC Cancer volume 13, Article number: 341 (2013)
The tumour suppressor and transcription factor p53 is a major determinant of the therapeutic response to anthracyclines. In healthy tissue, p53 is also considered pivotal for side effects of anthracycline treatment such as lesions in haematopoietic tissues like the spleen. We used a Trp53null mouse to explore the significance of p53 in anthracycline (daunorubicin) induced lesions in the spleen.
Mice with wild type or deleted Trp53 were treated with the daunorubicin (DNR) for three consecutive days. Spleens were collected at various time points after treatment, and examined for signs of chemotherapy-related lesions by microscopic analysis of haematoxylin-eosin or tunel-stained paraffin sections. Expression of death-inducing proteins was analysed by immunoblotting. Changes between Trp53 wild type and null mice were compared by t-tests.
Signs of cell death (pyknotic nuclei and tunel-positive cells) in the white pulp of the spleen occurred earlier following DNR exposure in wt-mice compared to Trp53-null mice. While the spleen of wt-mice recovered to normal morphology, the spleen of the Trp53-null animals still had lesions with large necrotic areas and disorganised histologic appearance eight days after treatment. Immunoblotting showed that only Trp53-wt mice had significant increase in p21 after DNR treatment. However, both wt and null mice had elevated p63 levels following DNR exposure.
p53 protects against severe and enduring cellular damage of the spleen parenchyma after DNR treatment, and initial DNR-induced apoptosis is not predictive of tissue lesions in the spleen. Our data indicate that p53 induction following DNR treatment serves to protect rather than to destroy normal tissue.
Numerous studies have demonstrated that the efficiency of DNA-damaging drugs in cancer therapy is dependent on the cellular status of the tumour suppressor factor p53[1–4]. The p53 pathway is often inactivated in human cancers, and deletions and mutations in p53 are associated with progressive and more aggressive disease, and with poor prognosis and anthracycline resistance in several types of cancer [1, 4–6]. In line with these results, there has been an increased focus on developing new drugs aiming to restore p53 activity in tumours [7–12]. However, the effect of p53 activation by drugs such as the anthracyclines on healthy tissue has to be considered in this respect, as induction of cell death and tissue damage in healthy tissue is an unwanted and severe side-effect of the anthracyclines.
It is known that anthracyclines cause lesions in haematopoietic tissues . We therefore addressed the role of p53 in the toxic activity of the anthracycline daunorubicin (DNR) in the spleen, and compared the effect of DNR on the spleen in C57Bl/6 wild type (wt) and C57Bl6 Trp53-null mice. DNR induced more rapid cell death and loss of spleen weight in wild type (wt) compared to Trp53-null mice. However, whereas the Trp53-null mice had severe lesions of the spleen at day 4 after treatment, there was spleen structure recovery in Trp53-wt animals. Our data points to p53 as a protective factor in chemotherapy-induced normal tissue damage.
The Trp53-null mouse was generated by Jacks et al. , and was provided by Prof. Lozano, MD Anderson Cancer Center, Houston, TX, USA. Trp53-wt and null mice (C57BL/6) were generated by litter-mate inbreeding. Genotypes of weaned mice were determined by PCR analysis of DNA from an ear biopsy .
The mice used were male, and age matched. DNR (Sanofi-Aventis, Lysaker, Norway,) was administered intravenously (10 mg/kg) through the tail vein for three consecutive days. Control animals received relevant vehicle. Health status and weight of the mice were monitored daily. The mice experiments were approved by the Norwegian Animal Research Authority and conducted according to the European Convention for the Protection of Vertebrates Used for Scientific Purposes.
Preparation and analysis of histological specimens
Spleens were excised from euthanized mice and washed in ice-cold PBS. Formalin-fixed tissues were embedded in paraffin, cut into 2-μm-thick sections and stained with haematoxylin and eosin (H&E). Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labelling (TUNEL staining, In situ Cell Death Detection Kit, POD, Roche) was used for in situ staining of apoptotic DNA fragmentation. Pyknotic nuclei and cells containing lipofuscin-like pigments were assessed by microscopy of H&E-stained paraffin sections. The number of pyknotic nuclei in all the white pulp areas was counted and then divided by the number of white pulp regions.
The spleens were cut with scissors and cell suspensions were prepared by crushing the tissue pieces between two glass slides in PBS. Cell suspensions were filtered through a nylon cell strainer (40 μm), washed in PBS by centrifugation (160 × g, 6 min) and re-suspended at 0.5 × 106 cells/ml in RPMI-1640 (Sigma-Aldrich Inc, St. Louis, MO) supplemented with 10% FCS (Gibco, Grant Island, NY). Cell death was assessed by flow cytometry after AlexaFluor 647-AnnexinV (Molecular Probes, Eugene, OR) and propidium iodide (PI) labelling. At least 30 000 non-gated live cell events were collected for each sample on an AccuriC6 cytometer (Ann Arbor, MI). Cells positive for AnnexinV alone or together with PI were counted as dead (apoptotic or necrotic). Untreated cells had less than 15% spontaneous cell death, and this was subtracted from the data on anthracycline-treated cells.
The data was compared by one-way analysis of variance (ANOVA) using IBM SPSS Statistics for Mac (version 19.0; IBM Corp.: Armonk, NY, 2010).
Protein lysates were prepared from excised spleens, snap-frozen in liquid N2 and stored at -80°C. Tissue was grinded with a pestle and lysed in RIPA buffer supplemented with Complete mini protease inhibitor (Roche Diagnostics, Mannheim, Germany). The relative protein concentration was determined by Bradford and adjusted by Coomassie staining, and immunoblotting was as described . Primary antibodies were from Santa Cruz Biotechology (Santa Cruz, CA, USA; p21, p63, Bax), and Imgenex (San Diego, CA, USA; p73) and secondary alkaline-phosphatase-conjugated antibody (a-3687 and a-3562) were from Sigma. CDP-Star substrate was from Tropix (Bedford, MA, USA). Chemiluminescence was detected using a Luminescent Image Analyser Apparatus (LAS 3000, FujiFilm, Tokyo, Japan) and Image Gauge Software (FujiFilm, Tokyo, Japan).
Results and discussion
Since p53 status is often coupled to therapy response to anthracyclines like daunorubicin (DNR) and idarubicin (IDA) , we examined the effect of anthracyclines on splenocytes and spleen histology. We first studied if p53-status affected the in vitro response to the anthracyclines daunorubicin (DNR) and idarubicin (IDA) in cells isolated from the spleen, since p53 deficiency is often coupled to anthracycline resistance . Both DNR and IDA are used as part of the standard treatment regime in leukaemia. We found that both drugs induced cell death to a similar degree insplenocytes from both wt and Trp53-null mice (Figure 1A). Hence, lack of p53 did not significantly seem to render the splenocytes resistant to anthracycline-induced death in vitro.
We next studied the in vivo effect of DNR treatment on the intact spleen in wt and Trp53-null mice. A typical therapy regime for AML patients consists of multiple 1–3 hour infusions of DNR during 3–6 days . To study how p53 is involved in the drug-induced damage and recovery of the spleen, we administered DNR (10 mg/kg) i.v. to the mice every day for three days. Whereas spleen weight reduction was evident two days after onset of DNR-treatment in wt-mice (Figure 1B), in the Trp53-null mice reduced spleen weight was not observed until about five to six days after onset of treatment (Figure 1C). Also, weight reduction was more prominent in the wt mice compared to Trp53-null animals. A p53-dependent decrease in spleen mass has similarly been reported by others after ionising radiation . Two weeks after treatment, there was an increase in spleen weight in both wt- and Trp53-null mice treated with DNR (Figure 1B,C; right plot).
We suspected that the early reduction in spleen weight could be due to cell death in the spleen. Accordingly, we found two hallmarks of cell death in spleens from wt-mice: 4 hours after the last treatment, the white pulps were scattered with i) pyknotic nuclei (Figure 2A, left panel), which corresponded with an increase of ii) TUNEL-positive nuclei (Figure 2A, right panels). The presence of both pyknotic and TUNEL-positive nuclei decreased during the next 20 hours (Figure 2A). Spleens from Trp53-null mice had no cells with pyknotic or TUNEL-positive nuclei in the white pulp 4 or 24 hours after DNR treatment (Figure 2A), suggesting that this early cell death was p53-dependent. Hence, a late onset of spleen weight reduction in Trp53-null mice corresponds to lack of early induction of cell death.
However, when we studied spleens from 3 Trp53-wt and 4 -null mice 4 days after the last DNR injection, we found pyknotic nuclei and gross pathological lesions in histological sections in both red and white pulp of the spleen only in the Trp53-null mice (Figure 2B). At this time, the wt mice had established normal spleen morphology with little or no signs of cell death (Figure 2B). Thus a late wave of p53-independent cell death seems to appear in the spleen of the Trp53-null mice. This later wave of cell death coincides with decreased spleen weight (Figure 1C).
We also found signs of DNR-induced cell death in the red pulp of the wt-mice. An increasing number of cells containing lipofuscin-like pigments were detected 4 hours after the last DNR injection (Figure 2C). Elevated levels of lipofuscin-like pigments have been found in the spleen of mice subjected to ionising radiation , and could be due to accumulation of non-degradable debris in for instance macrophages . The number of cells positive for lipofuscin-like pigments decreased during the next 20 hours (Figure 2C), as was seen for pyknosis and TUNEL-positive cells (Figure 2A). Interestingly, Trp53-null mice had high numbers of cells containing lipofuscin-like pigments both in the red pulp (Figure 2C) and in the white pulps (not shown), and treatment with DNR did not increase the number of cells containing lipofuscin-like pigments (Figure 2C). This suggests that natural turnover of cells in the spleen of Trp53-null mice leave degradation products such as lipofuscin-like pigments.
Four hours after completed DNR treatment we also detected a 4–5 fold increase in the number of mature and maturing polymorphonuclear cells in the red pulp both in Trp53-wt and null mice (Figure 2D). Stem cells and progenitors have been reported to migrate between bone marrow and spleen after induction of haematopoietic cell stress . This migration could be a response to bone marrow deprivation after DNR treatment, and indicate that the spleen red pulp partly replaces haematopoietic functions after extensive DNR treatment.
The late wave of cell death that we observed in the Trp53-null mice (Figure 2B) has similarly been reported to occur in the intestine of the Trp53-null mice after gamma-irradiation and has been assigned to induction of mitotic catastrophe due to lack of p53-induced cell cycle arrest . We therefore analysed spleens from DNR-treated Trp53-wt and -null mice for p21 induction. Immunoblotting showed elevated expression of p21 in spleens from wt-mice at 24 and 48 hours after DNR treatment (Figure 3, left panel) similar to what is seen with other DNA-damaging agents [22, 23]. The Trp53 null mice had only modest increase in p21 levels (Figure 3, right panel). The early elevation in p21 in the spleen from wt-mice could offer protection against severe tissue damage by induction of transient cell cycle arrest that allows the cells to repair drug-induced DNA damage and hence protect against mitotic catastrophe.
p63 is, together with p73, shown to be crucial for p53-meidated cell death after DNA damage , and can increase Bax expression and sensitise cells to apoptotic stimuli . We found that p63 and to some degree Bax was elevated in spleens from wt-mice at 24 and 48 hours after DNR treatment (Figure 3), the same time points where there was an increase in apoptotic nuclei and lipofuscin-like pigments (Figure 2A and C). We did not find any change in the expression of p73 neither in Trp53-wt nor null mice (data not shown). The Trp53-null mice had a prolonged increase of p63 and Bax, which lasted until 96 hours after termination of DNR treatment (Figure 3). This coincides with the late wave of p53-independent cell death that appeared in the spleen of the Trp53-null mice. It thus appears that in addition to lack of early p21-mediated cell cycle arrest (eventually resulting in mitotic catastrophe), the late massive cell death seen in the spleen of Trp53-null mice (Figure 2B, right panel), but not in Trp53-wt mice (Figure 2B, left panel) could also be mediated by up-regulation of p63 and Bax in the absence of p53.
This report indicates an anthracycline-induced early p53-dependent cell death in the spleen. In the Trp53-wt mice, the spleen appeared to recover after DNR treatment with no histopathological signs of cell death or tissue deterioration present four days after end of treatment. However, Trp53-null mice suffered from large lesions in the spleen parenchyma corresponding to a later induction of p53-independent cell death. These findings have clinical implications for therapy aiming to restore p53-dependent cell death pathways in cancer cells with non-functional p53. The efficacy of this therapy approach is debated , and the response apparently varies between drugs . We show here that restoration of p53 activity does not damage the anthracycline-sensitive spleen, but may rather serve to protect this during intensive chemotherapy.
Wattel E, Preudhomme C, Hecquet B, Vanrumbeke M, Quesnel B, Dervite I, Morel P, Fenaux P: p53 mutations are associated with resistance to chemotherapy and short survival in hematologic malignancies. Blood. 1994, 84 (9): 3148-3157.
Peller S: Clinical implications of p53: effect on prognosis, tumor progression and chemotherapy response. Semin Cancer Biol. 1998, 8 (5): 379-387. 10.1006/scbi.1998.0100.
McCubrey JA, Abrams SL, Ligresti G, Misaghian N, Wong EW, Steelman LS, Basecke J, Troppmair J, Libra M, Nicoletti F, et al: Involvement of p53 and Raf/MEK/ERK pathways in hematopoietic drug resistance. Leukemia. 2008, 22 (11): 2080-2090. 10.1038/leu.2008.207.
Rucker FG, Schlenk RF, Bullinger L, Kayser S, Teleanu V, Kett H, Habdank M, Kugler CM, Holzmann K, Gaidzik VI, et al: TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome. Blood. 2012, 119 (9): 2114-2121. 10.1182/blood-2011-08-375758.
Aas T, Borresen AL, Geisler S, Smith-Sorensen B, Johnsen H, Varhaug JE, Akslen LA, Lonning PE: Specific P53 mutations are associated with de novo resistance to doxorubicin in breast cancer patients. Nat Med. 1996, 2 (7): 811-814. 10.1038/nm0796-811.
Weller M: Predicting response to cancer chemotherapy: the role of p53. Cell Tissue Res. 1998, 292 (3): 435-445. 10.1007/s004410051072.
Kojima K, Konopleva M, Samudio IJ, Shikami M, Cabreira-Hansen M, McQueen T, Ruvolo V, Tsao T, Zeng Z, Vassilev LT, et al: MDM2 antagonists induce p53-dependent apoptosis in AML: implications for leukemia therapy. Blood. 2005, 106 (9): 3150-3159. 10.1182/blood-2005-02-0553.
Peterson LF, Mitrikeska E, Giannola D, Lui Y, Sun H, Bixby D, Malek SN, Donato NJ, Wang S, Talpaz M: p53 stabilization induces apoptosis in chronic myeloid leukemia blast crisis cells. Leukemia. 2011, 25 (5): 761-769. 10.1038/leu.2011.7.
McCormack E, Haaland I, Venas G, Forthun RB, Huseby S, Gausdal G, Knappskog S, Micklem DR, Lorens JB, Bruserud O, et al: Synergistic induction of p53 mediated apoptosis by valproic acid and nutlin-3 in acute myeloid leukemia. Leukemia. 2011, 26 (5): 910-917.
Yu X, Vazquez A, Levine AJ, Carpizo DR: Allele-specific p53 mutant reactivation. Cancer Cell. 2012, 21 (5): 614-625. 10.1016/j.ccr.2012.03.042.
Morandell S, Yaffe MB: Exploiting synthetic lethal interactions between DNA damage signaling, checkpoint control, and p53 for targeted cancer therapy. Prog Mol Biol Transl Sci. 2012, 110: 289-314.
Saha MN, Jiang H, Yang Y, Zhu X, Wang X, Schimmer AD, Qiu L, Chang H: Targeting p53 via JNK pathway: a novel role of RITA for apoptotic signaling in multiple myeloma. PLoS One. 2012, 7 (1): e30215-10.1371/journal.pone.0030215.
Buc-Calderon P, Praet M, Ruysschaert JM, Roberfroid M: Increasing therapeutic effect and reducing toxicity of doxorubicin by N-acyl dehydroalanines. Eur J Cancer Clin Oncol. 1989, 25 (4): 679-685. 10.1016/0277-5379(89)90204-6.
Jacks T, Remington L, Williams BO, Schmitt EM, Halachmi S, Bronson RT, Weinberg RA: Tumor spectrum analysis in p53-mutant mice. Curr Biol. 1994, 4 (1): 1-7.
Gausdal G, Gjertsen BT, Fladmark KE, Demol H, Vandekerckhove J, Doskeland SO: Caspase-dependent, geldanamycin-enhanced cleavage of co-chaperone p23 in leukemic apoptosis. Leukemia. 2004, 18 (12): 1989-1996. 10.1038/sj.leu.2403508.
Mayer RJ, Davis RB, Schiffer CA, Berg DT, Powell BL, Schulman P, Omura GA, Moore JO, McIntyre OR, Frei E: Intensive postremission chemotherapy in adults with acute myeloid leukemia. Cancer and Leukemia Group B. N Engl J Med. 1994, 331 (14): 896-903. 10.1056/NEJM199410063311402.
Komarova EA, Chernov MV, Franks R, Wang K, Armin G, Zelnick CR, Chin DM, Bacus SS, Stark GR, Gudkov AV: Transgenic mice with p53-responsive lacZ: p53 activity varies dramatically during normal development and determines radiation and drug sensitivity in vivo. EMBO J. 1997, 16 (6): 1391-1400. 10.1093/emboj/16.6.1391.
Wilhelm J, Brzak P, Rejholcova M: Changes of lipofuscin-like pigments in erythrocytes and spleen after whole-body gamma irradiation of rats. Radiat Res. 1989, 120 (2): 227-233. 10.2307/3577710.
Crichton DN, Busuttil A, Price WH: Splenic lipofuscinosis in mice. J Pathol. 1978, 126 (2): 113-120. 10.1002/path.1711260210.
Goris H, Bungart B, Loeffler M, Schmitz S, Nijhof W: Migration of stem cells and progenitors between marrow and spleen following thiamphenicol treatment of mice. Exp Hematol. 1990, 18 (5): 400-407.
Komarova EA, Kondratov RV, Wang K, Christov K, Golovkina TV, Goldblum JR, Gudkov AV: Dual effect of p53 on radiation sensitivity in vivo: p53 promotes hematopoietic injury, but protects from gastro-intestinal syndrome in mice. Oncogene. 2004, 23 (19): 3265-3271. 10.1038/sj.onc.1207494.
Perez BA, Ghafoori AP, Lee CL, Johnston SM, Li Y, Moroshek JG, Ma Y, Mukherjee S, Kim Y, Badea CT, et al: Assessing the radiation response of lung cancer with different gene mutations using genetically engineered mice. Front Oncol. 2013, 3: 72-
Yoshihara Y, Wu D, Kubo N, Sang M, Nakagawara A, Ozaki T: Inhibitory role of E2F-1 in the regulation of tumor suppressor p53 during DNA damage response. Biochem Biophys Res Commun. 2012, 421 (1): 57-63. 10.1016/j.bbrc.2012.03.108.
Flores ER, Tsai KY, Crowley D, Sengupta S, Yang A, McKeon F, Jacks T: p63 and p73 are required for p53-dependent apoptosis in response to DNA damage. Nature. 2002, 416 (6880): 560-564. 10.1038/416560a.
Gressner O, Schilling T, Lorenz K, Schulze Schleithoff E, Koch A, Schulze-Bergkamen H, Lena AM, Candi E, Terrinoni A, Catani MV, et al: TAp63alpha induces apoptosis by activating signaling via death receptors and mitochondria. EMBO J. 2005, 24 (13): 2458-2471. 10.1038/sj.emboj.7600708.
Jackson JG, Pant V, Li Q, Chang LL, Quintas-Cardama A, Garza D, Tavana O, Yang P, Manshouri T, Li Y, et al: p53-mediated senescence impairs the apoptotic response to chemotherapy and clinical outcome in breast cancer. Cancer Cell. 2012, 21 (6): 793-806. 10.1016/j.ccr.2012.04.027.
Bunz F, Hwang PM, Torrance C, Waldman T, Zhang Y, Dillehay L, Williams J, Lengauer C, Kinzler KW, Vogelstein B: Disruption of p53 in human cancer cells alters the responses to therapeutic agents. J Clin Invest. 1999, 104 (3): 263-269. 10.1172/JCI6863.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/13/341/prepub
This work was supported by the Norwegian Cancer Society, Lillemor Grobsoks Legat for Cancer Research and Norwegian Western Regional Health Authorities. The authors wish to thank Ing. Nina Lied Larsen for TUNEL staining, Ing. Wenche Eilifsen and Line Wergeland for animal maintenance. Flow cytometry was at Flow Cytometry Core Facility, University of Bergen, and histological sectioning and staining was performed at the Gade Institute and the Molecular Imaging Center (Fuge, Norwegian Research Council), University of Bergen.
The authors declare that there are no competing interests.
LH and GG: Designed the study and executed mouse experiments, cell death study and histopathological analyses. Prepared manuscript draft. LM: Designed and executed WB analyses, drafted manuscript. SOD and BTG: Study design, data interpretation and drafted manuscript. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Herfindal, L., Myhren, L., Gjertsen, B.T. et al. Functional p53 is required for rapid restoration of daunorubicin-induced lesions of the spleen. BMC Cancer 13, 341 (2013). https://doi.org/10.1186/1471-2407-13-341