- Open Access
Imaging biochemistry: applications to breast cancer
Breast Cancer Research volume 3, Article number: 36 (2000)
The use of magnetic resonance spectroscopy (MRS) to investigate breast tumour biochemistry in vivo is reviewed. To this end, results obtained both from patients in vivo and from tumour extracts and model systems are discussed. An association has been observed between transformation and an increase in phosphomonoesters (PMEs) detected in the 31P MRS spectrum, as well as an increase in choline-containing metabolites detected in the 1H spectrum. A decrease in PME content after treatment is associated with response to treatment as assessed by tumour volume. Experiments in model systems aimed at understanding the underlying biochemical processes are presented, as well as data indicating the usefulness of MRS in monitoring the uptake and metabolism of some chemotherapeutic agents.
The purpose of this section is to review the potential applications of magnetic resonance spectroscopy (MRS) to non-invasive probing of the underlying biochemistry of cells comprising a breast tumour. MRS does not generate an image of the tumour directly, but the spectroscopic data can now be obtained from a well localised area. Thus the biochemical information obtained from MRS can be interpreted in relation to a defined anatomical location, and images of metabolite distributions can be generated. In using MRS, the first aim is to identify surrogate biochemical markers of cellular transformation, thus differentiating benign tumours from malignant or potentially identifying the different tumour types. Subsequently, prognostic and diagnostic information is sought from the spectrum of malignant tumours. In prognosis, by yielding biochemical information on the tumour composition (eg the presence of a hypoxic or a drug-resistant fraction), MRS could allow the selection of an appropriate treatment. In diagnosis, early detection of tumour response to treatment, or monitoring of drug uptake and metabolism, could enable rapid optimisation of treatment if the tumour failed to respond. Overall, treatment that is better adapted to the individual patient could result from a better understanding of the biochemical events occurring within the tumour.
So far, most patient and model system studies have focused on 31P MRS. Within the 31P spectrum, the three nucleoside triphosphate (NTP) peaks, composed primarily of ATP, together with the inorganic phosphate (Pi) and phosphocreatine peaks, are indicative of energetic status. The Pi peak can also serve as a measure of intracellular pH. The phosphomonoester (PME) signal, which can be resolved into phosphocholine (PC) and phosphoethanolamine (PE) at higher field strengths or by decoupling, together with the phosphodiester (PDE) peak, composed of glycerol phosphocholine (GPC) and glycerol phosphoethanolamine, are indicative of lipid metabolism. Finally, NAD(H) and uridine diphosphate sugars can also sometimes be resolved in the 31P spectrum (Fig. 1).
In spite of its higher sensitivity compared to 31P MRS, 1H MRS has been used less frequently owing to the large signals from water and lipids that often dominate the spectrum, as well as the significant number of metabolite signals distributed over a relatively small chemical shift range. Nevertheless, when water-suppressed spectra are recorded, total choline, total creatine, lipids, glutamate, glutamine, inositols and lactate can be detected, potentially providing diverse biochemical information.
Other nuclei of interest include 19F and 13C. 19F has been used primarily in studies of drug metabolism, particularly 5-fluorouracil (5-FU). The use of 13C MRS in breast cancer has been restricted to model system investigations in which studies of the metabolism of specific pre-labelled compounds such as glucose or choline can be used to elucidate specific alterations in tumour biochemistry.
Considering spectra obtained from patients, these are often of poor sensitivity and resolution owing to technical challenges, the limited sensitivity of the method and low metabolite concentations. Consequently, the number of in vivo patient MRS studies is relatively limited, particularly in breast tissue. To identify the potential uses of MRS in the imaging of biochemistry in vivo, results obtained at higher field strengths from breast cancer tumour extracts will be discussed. Data obtained from model systems composed of homogenous cell populations or implanted tumour xenografts will also be presented, concentrating wherever possible on human breast cancer models.
Studies of tumour extracts, cells and xenograft models
Use of MRS to differentiate between benign and malignant tumours
In an effort to differentiate between benign and malignant tumours, early work concentrated on the 31P MRS spectrum of human breast tumour extracts [1*,2]. These studies demonstrated higher levels of PMEs and NTPs in the carcinomas relative to benign tumours. Others have identified an association between the PC component of the PMEs and tumour grade as well as the proliferating fraction [3,4]. The importance of the PME region in identifying cellular transformation was further recognised by pattern recognition studies of spectra obtained from xenografts and compared with normal tissues such as liver, brain or muscle . More recent studies comparing a normal human mammary epithelial cell line and a transformed human breast cancer cell line demonstrated that the levels of PMEs as well as PDEs were extremely low in the normal cells, and significantly less than in the breast cancer cell line . A further assessment of PC as well as total choline content in a series of breast cancer cell lines demonstrated that levels of choline-containing metabolites are correlated with malignant transformation and progression  as well as the acquisition of a metastatic potential .
Such studies have recently been complemented by 1H MRS investigations of extracts from non-involved breast tissue and breast tumours. The spectra demonstrated a high choline content as well as low levels of glucose and increased levels of lactate in the tumour spectra [8*]. Finally, spectra from about 200 fine-needle aspirate samples have shown that the choline peak in the 1H spectrum could be used to distinguish between benign and malignant tumours with relatively high sensitivity and specificity .
Use of MRS in understanding tumour biochemistry
As recently reviewed [10*], it is still not entirely clear which are the metabolic changes that lead to the increased levels of PMEs observed in breast and other cancers. Changes have been hypothesised to be associated with an enhanced cell membrane synthesis, cellular growth, or nutrient availability, as well as with cell signalling by lipid hydrolysis. Nevertheless, some understanding of the biochemical processes involved has been obtained by 13C and 2H MRS, in combination with labelled metabolites such as choline [4,11]. In breast cancer cells, rapid choline transport into the cells has been demonstrated, probably explaining the high levels of PC present in those cells. Furthermore, PC synthesis in quiescent breast cancer cells was slower than in proliferating cells, leading to lower PC levels in the non-proliferating population .
The rates of glucose uptake and lactate production have also been monitored with 13C MRS and labelled glucose. Such studies demonstrate that the rate of glycolysis is affected by the proliferation state of the cell, as well as by hormone treatment, with glucose uptake reduced in quiescent cells and in cells treated with tamoxifen . In other cell models, cellular de-differentiation  as well as apoptosis  were associated with changes in glucose uptake and metabolism that were detectable by MRS.
The chemical shift of the Pi peak enables the determination of pH within a sample. With the use of this information, MRS has been highly instrumental in demonstrating that whereas the extracellular pH of a tumour is acidic, its intracellular pH is in fact neutral to alkaline, leading to a reversed pH gradient in the transformed cell [14,15]. This finding affects the potential usefulness of some chemotherapeutic agents that are designed for optimum activity in an acidic intracellular environment, and some studies aimed at altering the pH gradient have been reported . Another aspect of tumour physiology that can affect response to treatment, particularly radiotherapy, is oxygenation, and 19F MRS of perfluorocarbons can be used in some cases to assess the presence of hypoxic regions within a tumour .
Use of MRS in monitoring response to therapy
The response to chemotherapy of experimental tumour models has been reviewed by Steen  and Daly and Cohen . They show that untreated tumour growth was associated in several studies with an increase in the PME resonance and a decrease in the signal intensity of energy-rich metabolites. This trend is reversed after chemotherapy. After treatment and tumour shrinkage, a decrease in PME levels has been observed. Furthermore, an increase in NTP levels was reported after response to treatment and was termed by Steen tumour 'activation', a process potentially resulting from improved perfusion to the cells present in the residual shrinking tumour.
The use of MRS to detect the uptake and metabolism of the chemotherapeutic drugs themselves is also possible in some cases, as has been recently reviewed by Griffiths and Glickson . 5-FU, which contains the magnetic resonance (MR)-visible 19F nucleus, has been extensively investigated and with 19F MRS it is possible to identify the catabolites of 5-FU in the liver, and to detect the parent drug as well as small peaks originating from the various nucleotides and nucleosides of 5-FU within the tumour itself. 19F MRS has also been used to monitor the conversion of 5-fluorocytosine to 5-FU after transgene expression in a glioma model . Others have been able to detect the expression of a virally transfected gene by monitoring the subsequent MR-visible build-up of a new metabolite in the 31P MRS spectrum . Finally, some studies of specifically labelled drugs such as 13C-temozolamide have also been reported , demonstrating that this methodology could also be used to monitor drug pharmacokinetics in vivo.
Studies in vivo
Use of MRS in differentiating between benign and malignant tumours
Negnedank [22**] comprehensively reviewed the MRS studies in vivo performed on different types of human cancer. More recently, concentrating specifically on human breast cancer, Leach et al [23*] summarised the finding from nine different 31P MRS studies in vivo. In line with the results obtained in model systems and described above, investigations in vivo demonstrate large PME and PDE signals in proliferating breast tumours. In 80% of breast cancers, PME signals, composed of both PC and PE, were higher than in normal breast, and PDE signals were higher in 77% of investigated tumours. If the Pi peak is taken as an indicator of pH, these reviews of the literature also demonstrate that breast tumours, like other cancers, show a slightly alkaline pH shift relative to control tissue. More recently, 1H MRS studies performed in vivo have also demonstrated an increase in the choline metabolite peak, which reflects choline, PC and GPC levels. Roebuck et al [24**] and Kvistad et al  showed an increase in choline-containing metabolites in 70-80% of breast carcinomas, whereas only 14-18% of benign tumours demonstrated a detectable choline peak. However, choline was also detected in most breast-feeding volunteers.
Use of MRS in monitoring response to therapy
On the basis of the review by Leach et al [23*], response to therapy has been associated with a decrease in PME content in 14 of 17 patients, with all non-responding patients demonstrating an increase in PME levels. A further serial study by the same authors of 25 patients undergoing hormone, chemotherapy and radiotherapy treatments showed a significant correlation between a decrease in PME, PDE and total NTP levels and response to therapy as measured by a decrease in tumour volume [23*]. A multi-institutional trial is now in progress to confirm these results by extending localised 31P MRS studies to investigate greater numbers of patients .
Considering the use of MR-visible chemotherapeutic drugs to monitor their uptake by the treated tumour, Wolf et al  recently published results obtained from different tumour types, including 26 cases of breast carcinoma. These studies demonstrated that after a bolus infusion of 5-FU, 'trapping' of the drug within the tumour region for relatively long periods (compared with drug in the blood pool) was strongly associated with tumour response to treatment, with 70% of trappers responding to treatment. None of the non-trappers demonstrated response to treatment.
The results obtained from tumour extracts, cell models and models of implanted xenografts demonstrate the potential of MRS in assessing surrogate markers of transformation and response to therapy. However, clinical measurements so far have often been limited by the signal : noise ratio as well as the length of time required for measurements. Nevertheless, considerable progress has recently been made in this area. Improved automatic shimming and calibration methods lead to shorter examination times and therefore make spectroscopic studies more acceptable to the patient. The implementation of decoupling in the 31P spectra has already led to an improvement in the separation of PE and PC signals in vivo as well as an improvement in signal : noise ratio by providing enhancement by the nuclear Overhauser effect. Recent measurements showing the practicality of 1H spectroscopy in the breast indicate the potential to measure smaller tumours in vivo than has been possible with 31P spectroscopy at 1.5 T. This also facilitates integrating such measurements into routine imaging studies because the same coil can be used. Most recently, new developments leading to clinical spectrometers with higher fields should improve both the sensitivity and the resolution of spectra in vivo. Together with improved localisation techniques, the ability to acquire signal from smaller voxels should lead to a better separation of tumour and normal tissue, and future studies might be able to generate enough metabolic information to provide both the diagnostic and prognostic parameters required by the clinician.
Degani H, Horowitz A, Itzchak Y: Breast tumors: Evaluation with P-31 MR spectroscopy. Radiology. 1986, 161: 53-55.
Merchant TE, Gierke LW, Meneses P, Glonek T: 31P magnetic resonance spectroscopic profiles of neoplastic human breast tissues. Cancer Res. 1988, 48: 5112-5118.
Smith TAD, Bush C, Jameson C, Titley JC, Leach MO, Wilman DEV, McCready VR: Phospholipid metabolites, prognosis and proliferation in human breast carcinoma. NMR Biomed. 1993, 6: 318-323.
Degani H, Ronen SM, Furman-Haran E: Breast cancer: spectroscopy and imaging of cells and tumors. In NMR in Physiology and Biomedicine. Edited by Gillies RJ. San Diego: Academic Press;. 1994, 329-352.
Howells SL, Maxwell RJ, Howe FA, Peet AC, Stubbs M, Rodrigues LM, Robinson SP, Baluch S, Griffiths JR: Pattern recognition of 31P magnetic resonance spectroscopy tumour spectra obtained in vivo. NMR Biomed. 1993, 6: 237-241.
Aboagye EO, Bhujwalla ZM: Malignant transformation alters membrane choline phospholipid metabolism of human mammary epithelial cells. Cancer Res. 1999, 59: 80-84.
Bhujwalla ZM, Aboagye EO, Gillies RJ, Chacko VP, Mendola CE, Backer JM: Nm23-transfected MDA-MB-435 human breast carcinoma cells form tumors with altered phospholipid metabolism and pH: a 31P nuclear magnetic resonance study in vivo and vitro. Magn Reson Med. 1999, 41: 897-903. 10.1002/(SICI)1522-2594(199905)41:5<897::AID-MRM7>3.3.CO;2-K.
Gribbestad IS, Petersen SB, Fjosne HE, Kvinnsland S, Krane J: 1H NMR spectroscopic characterization of perchloric acid extracts from breast carcinomas and non-involved breast tissue. NMR Biomed. 1994, 7: 181-194.
Mackinnon WB, Barry PA, Malycha PL, Gillett DJ, Russell P, Lean CL, Barraclough BH, Bilous M, Mountford CE: Fine-needle biopsy specimens of benign breast lesions distinguished from invasive cancer ex vivo with proton MR spectroscopy. Radiology. 1997, 204: 661-666.
Podo F: Tumour phospholipid metabolism. NMR Biomed. 1999, 12: 413-439. 10.1002/(SICI)1099-1492(199911)12:7<413::AID-NBM587>3.3.CO;2-L.
Katz-Brull R, Degani H: Kinetics of choline transport and phosphorylation in human breast cancer cells; NMR application of the zero trans method. Anticancer Res. 1996, 16: 1375-1379.
Ronen SM, Volk A, Mispelter J: Comparative NMR study of a differentiated rat hepatoma and its dedifferentiated subclone cultured as spheroids and as implanted tumors. NMR Biomed. 1994, 7: 278-282.
Ronen SM, DiStefano F, McCoy CL, Robertson D, Smith TAD, Al-Saffar NM, Titley J, Cunningham DC, Griffiths JR, Leach MO, Clarke PA: Magnetic resonance detects metabolic changes associated with chemotherapy-induced apoptosis. Br J Cancer. 1999, 80: 1035-1041. 10.1038/sj.bjc.6690459.
Griffiths JR: Are cancer cells acidic?. Br J Cancer. 1991, 64: 425-427.
Gillies RJ, Bhujwalla ZM, Evelhoch J, Garwood M, Neeman M, Robinson SP, Sotak CH, Van der Sanden B: Applications of magnetic resonance in model systems: Tumor biology and physiology. Neoplasia. 2000, 2: 139-151. 10.1038/sj.neo.7900076.
Evelhoch JL, Gillies RJ, Karczmar GS, Koutcher JA, Nalcioglu O, Raghunand N, Ronen SM, Ross BD, Swartz HM: Applications of magnetic resonance in model systems: cancer therapeutics. Neoplasia. 2000, 2: 152-165. 10.1038/sj.neo.7900078.
Steen RG: Response of solid tumors to chemotherapy monitored by in vivo 31P magnetic resonance spectroscopy: a review. Cancer Res. 1989, 49: 4075-4085.
Daly PF, Cohen JS: Magnetic resonance spectroscopy of tumors and potential in vivo clinical applications: a review. Cancer Res. 1989, 49: 770-779.
Griffiths JR, Glickson JD: Monitoring pharmacokinetics of anticancer drugs: non-invasive investigation using magnetic resonance spectroscopy. Adv Drug Deliv Rev. 2000, 41: 75-89. 10.1016/S0169-409X(99)00057-5.
Stegman LD, Rehemtulla A, Beattie B, Kievit E, Lawrence TS, Blasberg RG, Tjuvajev JG, Ross BD: Noninvasive quantitation of cytosine deaminase transgene expression in human tumor xenografts with in vivo magnetic resonance spectroscopy. Proc Natl Acad Sci USA. 1999, 96: 9821-9826. 10.1073/pnas.96.17.9821.
Walter G, Barton ER, Sweeney HL: Noninvasive measurement of gene expression in skeletal muscle. Proc Natl Acad Sci USA. 2000, 97: 5151-5155. 10.1073/pnas.97.10.5151.
Negendank W: Studies of human tumors by MRS: a review. NMR Biomed. 1992, 5: 303-324.
Leach MO, Verrill M, Glaholm J, Smith TAD, Collins DJ, Sharp JC, Ronen SM, McCready VR, Powles TJ, Smith IE: Measurements of human breast cancer using magnetic resonance spectroscopy: a review of clinical measurements and a report of localized 31P measurements of response to treatment. NMR Biomed. 1998, 11: 314-340. 10.1002/(SICI)1099-1492(1998110)11:7<314::AID-NBM522>3.0.CO;2-Z.
Roebuck JR, Cecil KM, Schnall MD, Lenkinski RE: Human breast lesions: characterization with proton MR spectroscopy. Radiology. 1998, 209: 269-275.
Kvistad KA, Bakken IJ, Gribbestad IS, Ehrnholm B, Fjosne HE, Haraldseth O: Characterization of neoplastic and normal human breast tissues with in vivo 1 H MR spectroscopy. J Magn Reson Imaging. 1999, 10: 159-164. 10.1002/(SICI)1522-2586(199908)10:2<159::AID-JMRI8>3.0.CO;2-0.
Arias-Mendoza F, Brown TR, Charles HC, Zakian K, Schwarz A, Doyle V, Nelson SJ, Rijkema M, Glickson JD, Evlehoch JL: Methodological standardization for a multi-institutional in vivo trial of localized 31P MR spectroscopy in human cancer research [abstract]. Proc Int Soc Magn Reson Med. 1999, 3: 1585-
Wolf W, Waluch V, Presant CA: Non-invasive 19F-NMRS of 5-fluorouracil in pharmacokinetics and pharmacodynamic studies. NMR Biomed. 1998, 11: 380-387. 10.1002/(SICI)1099-1492(1998110)11:7<380::AID-NBM517>3.0.CO;2-Q.
Smith TAD, Glaholm J, Leach MO, Machin L, Collins DJ, Payne GS, McCready VR: A comparison of in vivo and in vitro 31P NMR spectra from human breast tumours: variations in phosphlipid metabolism. Br J Cancer. 1991, 63: 514-516.
About this article
Cite this article
Ronen, S.M., Leach, M.O. Imaging biochemistry: applications to breast cancer. Breast Cancer Res 3, 36 (2000). https://doi.org/10.1186/bcr268
- magnetic resonance spectroscopy (MRS)
- 31P MRS
- 1H MRS